clinical research organization companies

Top 17 Clinical Research Organizations (CRO) in 2023

In clinical research and treatment development, clinical research organizations (CROs) are frequently a sponsor’s most important partner and ally.

Depending on the nature of the clinical trial, and your existing capabilities as a sponsor to run the trial, the CRO company of your choice will typically be responsible for facilitating most of the micro and macro processes that go into designing and running a successful clinical trial.

When contracting a CRO to help you with your trial, you are transferring over a large portion of responsibility into the hands of your clinical research partner. The CRO of your choice will have the responsibility to control a variety of factors and processes of a clinical trial, and depending on their expertise, team structures, service offerings, internal resources and many other capabilities.

Your ability to find and contract a top CRO company that is the right fit for your unique trial will be a determinant of whether or not you will be able to operate a high-quality clinical trial that meets your expected timelines, budget and delivers a top-notch patient experience.

At ClaraHealth (a patient-centric recruitment acceleration platform) , we have put together an extensive list of the top CRO companies in the US and around the world.

This is not a cro rankings list, but rather a compiled list of some of the top clinical research organizations around the world. We have highlighted their strengths and core service offerings to make it easier for you to find the right fit clinical research partner.

In addition, we’ve put together a list of 9 fundamental questions to ask the prospective clinical research organization , which will help you to save time and ensure a right fit in picking the CRO.

Formerly known as Quintiles and IMS Health, IQVIA is one of the largest CROs in the world, with a large range of service offerings to help advance clinical research.

The company was founded in North Carolina in 1982, and has since grown to over 88,000 employees in more than 100 countries.

Some clinical trial solutions offered by IQVIA include:

• Assistance with protocol design
• Design of phase 1 clinical trials
• Assessment and improvement of phase 2 and 3 clinical trials
• Site identification & selection
• Patient recruitment
• Access to global laboratories via their wholly owned subsidiary Q2 Solutions

Parexel is a global clinical research organization that was founded in 1982, and specializes in conducting clinical studies on behalf of its pharmaceutical partners in order to accelerate and ensure the drug approval process of up-and-coming potential treatments. It currently operates in more than 50 countries, and is run by more than 18,000 employees around the world.

The company has a wide range of service offerings, covering nearly every type of clinical trial service to assist sponsors in running successful clinical studies.

Some clinical trial solutions offered by Parexel include:

• Clinical trial design and development for early phase, phase 2 & 3, and late phase clinical trials
• Clinical data management
• Decentralized clinical trials
• Clinical supply chain management
• Medical writing
• Regulatory affairs consulting
• Pharmacovigilance

3. PRA Health Sciences

PRA Health Sciences is one of the largest contract research organizations in the world. Founded in 1976 under the name “Anti-Inflammatory Drug Study Group”, the company was renamed to PRA in 1982. PRA Health Sciences employees more than 17,000 people, and provides coverage to more than 90 countries.

In 2021, PRA Health Sciences was acquired by the Ireland-headquartered global CRO leader ICON, which is also reviewed in this list.

Some clinical trial solutions offered by PRA Health Sciences include:

• Decentralized Clinical Trials Platform
• Protocol Consultation & Study Design
• Onsite Support services
• Customized Solutions for Biotech (such as asset valuation, regulatory strategy, engagement and support, drug development strategy and funding solutions)
• Clinical Diagnostics
• Site Commercial Solutions
• PRA’s Laboratories for Drug Development

Headquartered in Ireland, ICON was founded in 1990 in Dublin by co-founders John Climax and Ronan Lambre. The company has since grown to be one of the largest CROs in the world. As of September 2020, the company employs more than 15,000 people in 94 locations and across 40 countries.

ICON offers clinical research services which include consulting, clinical development and commercialization across a wide range of therapeutic areas.

In 2021, ICON acquired PRA Health Sciences, which is another CRO and global leader in clinical research services.

Some clinical trial solutions offered by ICON:

• Commercial Positioning
• Early Phase
• Functional Services Provision
• Laboratories
• Language Services
• Medical Imaging
• Real World Intelligence
• Site & Patient Solutions
• COVID-19 Clinical Operations

5. Syneos Health

Formerly known as InVentiv Health Incorporated and INC Research, Syneos Health is a publicly listed and global contract research organization. The company is based in Morrisville, North Carolina, and specializes in assisting companies with late-stage clinical trials. Syneos Health currently employs more than 25,000 people, and has offices across 91 locations.

In early 2018, INC Research was acquired inVentiv Health, and the merged company was named Syneos Health.

Some clinical trial solutions offered by Syneos Health include:

• Decentralized Clinical Trials Solutions
• Bioanalytical Solutions
• Phase II-III/Phase IIIb-IIIV
• Medical Device Diagnostics
• Clinical Data Management
• Clinical Project Management
• Clinical Monitoring
• Drug Safety & Pharmacovigilance
• Site and Patient Access

6. Labcorp Drug Development (Formerly Covance)

Formerly known as Covance and renamed to Labcorp Drug Development in early 2021, this CRO is one of the largest contract research organizations in the world. The company claims to provide the world’s largest central laboratory network, and has been rated as one of the best places to work for LGBTQ+ equality by the Human Rights Campaign organization in 2018 to 2021. Currently, Labcorp employs over 70,000 people and is able to support clinical research efforts in almost 100 countries around the world.

Some clinical trial solutions offered by Labcorp Drug Development include:

• Preclinical Services
• Clinical Trials
• Clinical Trial Laboratory Services
• Post-Marketing Solutions
• Medical Devices
• Data & Technology

Also known as Pharmaceutical Product Development, PPD is a large global contract research organization headquartered in Wilmington, North Carolina. Started as a one-person consulting firm in 1985, PPD has grown to over 27,000 employees worldwide, and provides a wide range of clinical research services to pharmaceutical and biotech companies.

Some clinical trial solutions offered by PPD include:

• Clinical Development
• Early Development
• Peri- and Post-Approval
• PPD Biotech
• PPD Laboratories
• Product Development and Consulting
• Site and Patient Centric Solutions

8. Fisher Clinical Services

Part of Thermo Fisher Scientific, Fisher Clinical Services is a global clinical research organization with headquarters in Center Valley, Philadelphia.

The company has been in the business of clinical supply chain management for over 20 years, and is focused exclusively on working with the packaging and distribution requirements of clinical trials across the globe.

Some clinical trial solutions offered by Fisher Clinical Services include:

• Biologistics Management
• Cell & Gene Therapy
• Clinical Ancillary Management
• Clinical Label Services
• Clinical Trial Packaging & Storage
• Clinical Supply Optimization Services
• Cold Chain Management & Expertise
• Direct-to-Patient
• Distribution & Logistics
• Strategic Comparator Sourcing
• Public Health Research

Established in 1997 under the name Kiecana Clinical Research, KCR is a full-service contract research organization that provides a variety of services for clinical monitoring, safety & pharmacovigilance, clinical project management, quality assurance and regulatory affairs.

KCR operates globally, and has offices in North America, Western Europe, Central Europe and Eartern Europe. The company currently employs more than 700 staff.

Some clinical trial solutions offered by KCR include:

• Trial Execution

10. Medpace

Founded in 1992 and based in Cincinnati, Ohio, Medpace is a midsize clinical contract research organization. The company has operations in over 45 countries, and employs over 2,800 people. Medpace provides support services for Phase I-IV clinical trials for pharmaceutical and biotechnology companies, which include central laboratory services and regulatory services.

Some clinical trial solutions offered by Medpace include:

• Biostatistics and Data Sciences
• Clinical Trial Management
• Drug Safety and Pharmacovigilance
• Medical Writing
• Quality Assurance
• Regulatory Affairs
• Risk-Based Monitoring
• Medpace Laboratories

11. Clintec

Now in business for over 22 years, Clintec is a medium-sized global contract research organization for pharmaceutical, biotech and medical device industries, with large expertise in oncology and rare diseases.

The company provides the flexibility and agility of a smaller-sized CRO, while also having a wide global coverage that large CRO companies are known for. Clintec is based in more than 50 countries, and was acquired by the leading global CRO IQVIA in late 2018.

Some clinical trial solutions offered by Clintec include:

• Project Management
• Data Management
• Biostatistics
• Global Feasibilities
• Patient Recruitment & Retention

12. Worldwide Clinical Trials

Bringing over 30 years of experience to the clinical research market, Worldwide Clinical Trials is a leading medium-sized global contract research organization. Founded by physicians with a dedication and commitment to advancing medical research, Worldwide Clinical Trials was the first customer-centric CRO.

Currently the company has coverage in more than 60 countries, and has extensive experience in a wide range of therapeutic areas, including central nervous system, metabolic, cardiovascular, oncology, rare diseases and general medicine.

Some clinical trial solutions offered by Worldwide Clinical Trials include:

• Bioanalytical Lab
• Early Phase Development
• Clinical Phase IIB-II Clinical Trials
• Phase IIIB-IV Clinical Trials
• Trial Management Technologies

Named #1 CRO in the world for operational excellence at the 2021 CRO Leadership Awards, CTI Clinical Trial And Consulting Services is a medium-sized global contract research organization that has been serving pharmaceutical companies since 1999.

Based in Covington, Kentucky, CTI has offices around the world in more than 60 countries, with coverage in North America, Europe, Latin America, Middle-East, Africa, and Asia-Pacific regions.

Some clinical trial solutions offered by CTI include:

• Feasibility
• Regulatory Affairs Study Start-Up
• Medical Monitoring
• Safety & Pharmacovigilance
• Clinical Services

14. Wuxi AppTec

Founded in 2000 as WuXi PharmaTech in the city of Wuxi, China, Wuxi AppTec has grown from a single laboratory into a leading global contract research organization with more than 28,000 employees, including 23,000 scientists and more than 30 research & development and manufacturing sites around the world.

With offices in Asia, U.S, Europe and the Middle East, the company is able to provide coverage to more than 30 countries around the world.

Some clinical trial solutions offered by Wuxi AppTec include:

• Small Molecule Drug R&D and Manufacturing
• Cell Therapy and Gene Therapy
• Drug R&D and Medical Device Testing
• Clinical Services (Phase I-IV)

15. Advanced Clinical

Founded in 1994 and based out of Deerfield, Illinois, Advanced Clinical is a midsize and full-service CRO that helps sponsors with running clinical trials. The company employs more than 700 staff, and offers a wide variety of services across many therapeutic areas. Advanced Clinical has global representation in over 50 countries around the world.

Some clinical trial solutions offered by Advanced Clinical include:

• eTMF & Document Management
• Global Medical Services
• Quality & Validation

16. Pharm-Olam

Pharm-Olam is a leading midsize CRO with global headquarters located in Houston, Texas and its European headquarters in Bracknell, United Kingdom. The company employs more than 800 staff, and has 25 offices around the world, with a global coverage in more than 60 countries.

The company has therapeutic expertise in 5 areas, including Rare & Orphan Disease, Infectious Disease & Vaccine, Oncology-Hematology, Allergy and Autoimmune.

Some clinical trial solutions offered by Pharm-Olam include:

• Study Feasibility
• Site Activation
• Patient Recruitment
• Medical Affairs
• Compliance & Training
• Clinical Monitoring & Operations

17. Clinipace

Founded in 2003 and based out of Morrisville, North Carolina, Clinipace is a global midsize full-service CRO with a focus on solution customization for clinical trials. The company has a large global coverage in more than 50 countries, and has offices in North America, South America, Europe and Asia-Pacific regions.

Clinipace’s therapeutic focus areas include Oncology, Nephrology and Urology, Rare Disease, Gastroenterology and Women’s Health. The company also has complete therapeutic expertise in Infectious Disease & Vaccines, Cardiology, CNS, Immunology, and Respiratory.

Some clinical trial solutions offered by Clinipace include:

• Clinical Analytics
• Clinical Technology and Ecosystem
• Functional Service Partnership (FSP)
• Regulatory & Strategic Product Development

9 Fundamental Questions To Ask A Top CRO Company Before Signing The Contract

1. which services does the cro provide.

CROs offload a lot of operational tasks from trial sponsors, which can touch any component of clinical trial operations. From formulating an overall study strategy and implementing technologies to support the operational processes of the trial, to picking and identifying sites, and supporting patients during the trial, the range of clinical services offered by a CRO tends to be vast and inclusive of all the typical services and support you will require for running a successful clinical trial.

However, not all CROs are the same in their service offerings, or are able to offer the same depth of capability within a seemingly same clinical trial support process. For this reason it is important to understand exactly which kind of clinical services and support you are looking to receive from the prospective CRO when running your clinical trial.

While services such as clinical monitoring and clinical trial management are offered by the majority of CROs, the specific needs of each trial are unique, and for this reason it is important to first identify what will be the unique services your trial requires. Completing this internal analysis first will help you to understand the extent to which a potential CRO partner will be able to provide all of these services.

Some CROs specialize in specific clinical trial functions which the company may label as a “core services”, in which case this is a sign the company will have more expertise, experience, and will be set up in a way to maximize their capabilities in providing support for these services compared to other services that the CRO offers.

For example, a CRO may include patient recruitment as part of its “core services”, which implies that they are highly skilled in and have the necessary infrastructure to design and implement a high-quality patient recruitment strategy.

Clara Health CRO Support Services: At Clara Health our specialty services include technology-augmented digital and patient advocacy recruitment, as well as patient support via our signature patient recruitment platform, which we use to upgrade clinical trials and deliver results sponsors look for in their recruitment and retention campaigns.

At Clara, we work alongside CROs to supplement and support clinical trials with modern and personalized capabilities that CROs do not typically have the bandwidth, corporate structure or infrastructure to support.

If you would like to learn more about exactly how our platform can upgrade your unique trial, feel free to book a Free 30 Minute Consultation Session Here with one of our in-house experts.

2. What Related Experience Does The CRO Have?

It is helpful to ask the prospective CRO company if they have any relevant experience in running clinical trials that would be an asset in designing and running your study. Previous experience in a related therapeutic area or in running a trial with a similar design allows CROs to have a deeper understanding into potential opportunities and challenges, increasing the likelihood of your clinical study being successful.

For example, if a sponsor is planning to run a trial in oncology, for the purpose of site identification and selection it would be valuable to partner with a CRO vendor that has expertise in this area, as they likely already have a good understanding of which sites will lead to optimal results.

However, it is also important to consider all factors when selecting a CRO vendor and not to rely on therapeutic experience as the sole qualifier for whether or not a potential CRO is a fit for your trial. While previous experience is beneficial, some sponsors close themselves off from working with vendors that have not worked in their therapeutic area, which significantly limits options when choosing a CRO partner that is truly a good fit for their clinical study.

This can impact the end result of your clinical study, as sponsors that are not successful in choosing a CRO vendor that is the right overall fit may face difficulties if the needs of their clinical study aren’t being properly met.

Clara Health: We have worked to provide support for clinical trials across a wide range of therapeutic areas and trial designs. Our specialty is filling in the gaps that CROs traditionally did not have to think about, which include digital patient recruitment, patient advocacy recruitment, and technology-augmented patient support.

Additionally, we are constantly building our proprietary data and running tests in a variety of therapeutic areas. These research efforts allow us to have a detailed understanding of the expected level of difficulty when recruiting particular patient populations, as well as allow us to predict with accuracy which segments of the targeted population will be likely to qualify in a particular study.

3. What Are The Communication Workflows & Expectations For Performing And Delivering Contracted Services?

It is important that you clarify what the expectations for communication will be between your prospective CRO vendor and your internal teams, as you will most likely be working with the CRO of your choice for the entire duration of your clinical trial.

There are a vast variety of factors and success determinants for a clinical trial, which are continuously undergoing change as the study unfolds. For this reason, it is recommended that you work with a CRO that is proactive in their communication, so that you are kept up to date with information about important changes as your clinical trial progresses.

A vendor that is proactive rather than reactive in their communication and approach to dealing with arising issues is one of the most important qualities in CRO. Challenging situations will naturally arise, and the promptness with which they are taken care of will significantly impact your clinical trial’s degree of success. Therefore, seeking a vendor that is able to match the standard of communication that you as a sponsor would like to experience throughout the duration of your partnership is one of the most critical steps in determining which CRO is the right fit for your clinical trial.

We’ve included a few additional questions pertaining to the communication structure and reporting expectations that you can ask a prospective CRO vendor to determine the degree of fit in this particular category:

Communication Expectations:

• If we were to move forward with you, which of your team members will be our main point of contact?
• How available will you be outside of the scheduled meetings to address any of our concerns or additional requests?
• What will be the frequency at which update meetings will be conducted, and who will be present at those meetings?
• Which clinical study processes will be reported on, and what will be the workflow for how we will receive this information?
• What will be the cadence at which we will receive progress reports?
• Would we be able to access metrics electronically via an interactive dashboard, or will you send us formal reports?

Clara Health: At Clara Health, we directly interact and actively work with several key stakeholders involved in running a clinical trial, which includes sponsors, CROs, sites, and patients. This unique position allows us to have a centralized perspective which helps us to see all the moving parts of a clinical trial at the same time, which helps to identify issues and relay this vital information and insight back to the sponsor (or other appropriate stakeholders) in the shortest time possible.

The ability to access this perspective allows us to gather the most accurate, complete, and up-to-date information about how the clinical trial is unfolding, and quickly becomes very valuable to sponsors for their clinical trial.

As an example, we may receive feedback from patients about having an unsatisfactory experience with a particular study site. We are able to aggregate and analyze this information, and relay our findings back to the sponsor and the study site to improve the experience for other patients.

4. What Is The CRO’s Client Satisfaction Record?

It is a good practice to request information or metrics from the prospective CRO vendor that can point to the degree of satisfaction of their past clients. Prior to signing the contract, vendors will naturally do their best to uplift their image and future value to you during their sales conversations with you and your team. It can be tricky to get an objective understanding of what the partnership experience will actually entail, especially when there are multiple vendors fighting for your commitment.

We recommend that you ask the prospective vendor to provide success metrics regarding areas of clinical trial operations that are going to be important for your trial.

For example, you may be interested in learning about the vendor’s relationship to finances, in which case it will be useful to ask them about situations in which they went over the planned budget, and investigate into the reasons behind that. Alternatively you may be concerned about potential delays in timelines, in which case it would be helpful to learn about metrics regarding the CRO’s ability to meet timeline expectations.

You may also request to talk to the prospective CRO’s past clients, which will help you to gain insight into what the relationship was like and give you the opportunity to examine if the way in which the particular CRO manages its relationships and performs its services meets the expectations that you would have for your potential relationship and for your clinical trial.

Clara Health: At Clara Health, our relationships with our partners and with our patients are most important to us. In the unique position where we fit in the clinical trial process, we have the opportunity to directly co-create the clinical trial patient experience with a variety of stakeholders, including sponsors, sites, CROs, and patients.

Our company’s values and culture have been directed and developed to be such that the client and patient experience is at the top of priority for all of our internal teams, and we work to provide the best quality of care to all stakeholders.

We have many testimonials from every type of partner we’ve worked with which we can happily share with you.

5. How Do You Adapt When Encountering Challenges With Running A Clinical Trial?

It is inevitable that challenges and unforeseen changes will arise throughout the operational clinical trial process, and for this reason it is important to work with a CRO vendor that can provide you with evidence of their flexibility and ability to adapt to sudden changes.

The ideal CRO partner is one that is highly consultative throughout the entire process, and has an ability and the initiative to deal with challenges at their seed stage, prior to them turning into major obstacles for the success of your trial.

CROs naturally have a large reach, and there are a lot of different clinical trial mechanisms and processes that are under their control. They are able to monitor and respond to what is going on in every key link in the chain of the clinical trial operation.

It is reasonable to expect this level of oversight from a CRO, and additional questions that can help you gain insight into this include:

• What are some examples where the CRO was effective at monitoring the health of clinical trials they’ve helped operate in the past?
• How quickly does the CRO respond to challenges or opportunities for improving the clinical trial experience?
• How well does the CRO gather & process information from study sites, study teams, patients & the sponsor, and what are their typical data analysis workflows?

It is also recommended to speak to the prospective CROs past clients to help you gain insight into how well they respond and adapt to the naturally arising challenges in clinical trials.

Clara Health: While CROs do have a large reach within the clinical trial, no CRO has complete visibility into every clinical process. They are not typically set up to support full visibility, which can manifest as a potential threat to your clinical trial as it unfolds. This is especially true for parts of the clinical trial processes that CROs naturally do not specialize and often subcontract, such as clinical trial recruitment.

At Clara, we are in a unique position in relation to other key partners involved in operating the clinical trial. We are in direct and frequent contact with patients, CROs, study sites, study teams, and the sponsor, and have a very deep understanding of the patient pipeline. This allows us the unique ability to go very deep into specific parts of the recruitment chain and investigate what is working and what is not working.

In addition, Clara functions as a resource for all partners in the clinical trial. For example, we work directly with site teams to ensure that they have access to a 3rd party that they can relay their needs to and receive fast support in case there is anything they require that can improve the patient recruitment process.

6. Which Parts Of Operating The Clinical Trial Will You Be Outsourcing?

Since there are so many processes and mechanisms that go into operating a clinical trial, CROs will always outsource some parts of running and managing the study. While you can expect that the prospective CRO will subcontract some of the work, it is important to find out which exact parts the clinical study will be outsourced.

There are certain basic and key clinical processes (such as site selection) that CROs almost always help with, and if you find that these parts of your trial are going to be subcontracted to another company, it is recommended to find out why the CROs operations are set up this way and how this would impact the service you will receive.

Ultimately what matters to you as a partner and client is that the quality of service and care that you will receive will be up to standard, and meet what was promised and what you are expecting. While this trust is important after you have signed the contract, it is recommended that prior to entering into such a significant commitment that you have evidence and the conviction that the CRO of your choice is truly the right fit and will deliver the quality of service that was being discussed.

Since it is impossible to predict exactly what the quality of this relationship and services performed will actually be like in practice, it is recommended that you understand the details of what will be done for your trial and how. Investigating how the CRO outsources and subcontracts services for a clinical trial will help you to gain necessary insight that you would need to make the correct vendor selection decision.

Clara Health: At Clara, we maximize the effectiveness of the digital component across the entire digital & recruitment spectrum, which is added on top of the existing capabilities of the CROs and other vendors involved in operating your clinical trial. In addition, we offer services that augment the CROs efforts, which has the potential to significantly improve the patient experience, operations flows, recruitment and retention performance, which is so important in ensuring the success of a clinical trial.

For example, if a CRO wants to have a great site relationship, we are able to come in as a third party on behalf of the sponsor and CRO and act as a resource and additional support for sites.

In another example, If a sponsor wants to have great relationships with the patient community, Clara is able to come in on behalf of the sponsor and develop these relationships while being perceived more neutrally by the patient community.

7. Do You Have Experience Running International Trials?

If you are planning on operating an international clinical trial, it is recommended to work with a CRO that has extensive experience in this area. While many CROs will offer near-global coverage, the level of experience with specific geographic locations can significantly vary from one vendor to another.

It is important to work with a CRO that has experience running clinical trials in the specific countries and regions you are planning to conduct your research in. Being compliant with the local rules and regulations for clinical testing is a very complex process that requires existing understanding and familiarity in order to ensure logistical smoothness and to mitigate legal risks. In operating a clinical trial, there are a multitude of clinical services and processes, which can greatly vary across the many regions in which you can conduct clinical testing.

A CRO that is lacking experience in operating international trials or operating in particular regions where you plan on conducting research may not be able to meet your desired quality and agility expectations, and therefore may not be the right fit for your international clinical trial.

Clara Health: In the past, we have provided international patient recruitment and digitally-augmented trial support services for clinical trials in the EU, Canada, UK, Australia and South America.

Clara Health is fully compliant to operate international studies everywhere in the world, with the exception of Russia and China.

8. What Is Your Relationship With Patients?

Patient-centric approach to designing and operating a clinical trial is becoming more and more crucial in the clinical research space. The ability of a sponsor and their CRO partner to understand the needs and characteristics of their target patient community is a significant determinant of whether or not the study will be a success.

A sponsor that has close and authentic relationships with the patient community tends to have a deeper understanding of how to create the best clinical trial experience that will attract patients and keep their interest throughout the clinical trial.

In addition, strong relationships with patients allow sponsors and CROs to forecast recruitment and patient retention pipeline with much higher accuracy. This ability is critical for ensuring the success of the trial and mitigating the risk of low enrollment. After an understanding of the patient population is acquired, sponsors gain the necessary insight to design a clinical trial that is not only favorable to their research results, but is also practical and will result in the enrollment numbers they are looking for.

While many CROs have already recognized the importance of patient-centricity and evolved the ways in which they design and operate clinical trials, other CROs have not yet made such a pivot in their values. It is important to understand the degree of importance the prospective CRO places on creating a favorable patient experience, and what kind of infrastructure the company has to support it.

At Clara, we recommend choosing a CRO partner that is adapting to the patient-centric model which is becoming more and more important for running a successful clinical trial.

Clara Health: Since early stages of our development, we’ve had a dedicated patient advocacy team that has been integral in shaping our company’s vision and operations. We have built our entire platform and recruitment infrastructure around creating the best experience for patients. Our teams, corporate values, service offerings and company infrastructure all work in the service of the patient.

In addition, over the many years of being in business we have heavily invested in building authentic patient community relationships that span across a variety of therapeutic areas. This has given us a unique ability to receive feedback directly from patients that is genuine and authentic around marketing materials, strategy for patient recruitment, and other services that we build for specific trials.

This ability to build partnerships with the patient community in an authentic way gives us a very unique ability to engage with the patient community on behalf of a pharmaceutical company, allowing our sponsor & CRO partners the opportunity to start conversations with patients through our in-house patient advocacy team.

If you would like to learn how Clara can help you to build a strong & authentic relationship with your target patient community, get in touch with us and we’d be happy to share our capabilities and previous results with you as they relate to your current or upcoming clinical trial.

9. How Is The CRO Going To Utilize Patient Input For Developing The Trial?

In the initial stages of clinical trial design, sponsors often determine the ideal patient profiles that would help them to drive the most favorable research outcomes for their study. While it is important for the success of your trial to determine who your ideal patients are, very often these projections do not match up with what is viable in practice.

At Clara, we often encounter study protocols that are not set up realistically for successful recruitment to be possible.

Common mistakes that are made when determining trial eligibility criteria and trial design include:

• Overestimating the interest in the clinical trial from the target patient population
• A lack of patient focus in the trial design
• A lack of convenience for patients in their participation
• Complicated and/or inefficient study experience flows
• Crafting the eligibility criteria around the patient population that is most likely to lead to favorable study outcomes, without conducting sufficient research to more accurately estimate the recruitment and retention difficulty of the group for a particular study

It is natural for there to be a “push & pull” between the research ideal and the real world practicality. It is important to determine the correct balance between these two sides for your trial, as going too far in either direction will decrease the chance of your clinical study’s success.

The nature of the industry as it is right now is such that there is excess research idealization and not enough emphasis on patient centricity. This distorted orientation has resulted in many clinical trials being unsuccessful, negatively impacting sponsors, patients and the entire clinical trials industry.

The ideal CRO partner should help you make sure that your protocol design sets your study up for success. The CRO should be able to help you determine the proper balance between the research ideal and the real world practicality, and back up their findings with sufficient research and patient data that can project your trial being a success.

Clara Health: When formulating a recruitment and retention plan for our clients, we begin with conducting thorough research into the target trial patient population. This allows us to get a clear understanding of which recruitment channels will yield the best results and what kind of marketing materials will resonate with the prospective study participants.

To ensure accuracy and real-world applicability of our research, we consult and collaborate with our internal patient advocacy and patient support teams, as well as with our clients and patients representing the target trial patient profiles. We then tie our findings back with any existing proprietary data that we have in connection with the therapeutic area or the prospective target patient group.

Our unique position within the clinical recruitment chain gives us the presence and deep-rooted access needed to effectively tap into any of the three patient traffic sources: digital recruitment, offline recruitment, or patient advocacy recruitment.

Once a recruitment campaign has gone live, we constantly monitor, analyze and optimize our performance to make sure that the processes we have in place are as efficient as possible and drive the greatest results. In addition, we have the capability to layer in any traditional advertising (such as billboard ads) if requested by the study sponsor.

The leading clinical research organizations

We've ranked the top 10 clinical research organizations.

UNBIASED RESEARCH RANKINGS

HIGHEST STANDARDS REQUIRED

PROPRIETARY CRITERIA SYSTEM

What people are saying: #Passionate #Innovative #Dedicated

Parexel is a clinical research organization that provides biopharmaceutical services and solutions. They have expertise in clinical development, translational medicine, and early phase research. Parexel has over 10,000 employees in 50 countries. Parexel has been recognized by Frost & Sullivan with the 2022 Global Customer Value Leadership Award. Parexel's services are designed to help pharmaceutical and medical device companies bring new treatments and therapies to market. Parexel's clinical development services include phase I-IV clinical trials, biostatistics, clinical data management, clinical supply chain management, decentralized clinical trials, medical monitoring and consulting, medical writing, patient sensors, pharmacovigilance, and risk-based quality management. The company's expanded access services provide access to investigational treatments for patients with serious or life-threatening conditions who are not eligible for clinical trials. Their outsourcing services include functional services provider and strategic partnerships.Parexel's team of experts has the knowledge and experience to help bring new treatments and therapies to market.

IQVIA clinical research

What people are saying: #Involved #ResearchOriented #PatientFriendly

IQVIA clinical research is a company that provides information on clinical trials and patient communities. They also have a section on their website where you can register for updates on new clinical trials and community events. The company has a strong focus on helping to expand meningitis research and they are currently recruiting participants for a new clinical study. They are also seeking volunteers to help advance respiratory syncytial virus (RSV) research. In addition, they are working on a clinical study to help find a way to speed up recovery from COVID-19 and reduce the need for hospital care. Overall, IQVIA clinical research is a company that is heavily involved in a variety of research studies in order to help improve medical treatments and find new cures for diseases.

What people are saying: #Comprehensive #Quality #Dedicated

Medpace is a full-service CRO that provides support for drug, biologic, and medical device programs. They have a global reach and offer services including clinical monitoring, biostatistics and data sciences, regulatory affairs, and more. They are dedicated to making the complex seamless and strive to provide the highest level of quality and service.

Syneos Health

What people are saying: #Quality #Experienced #Committed

Syneos Health is a biopharmaceutical company that provides solutions for clinical development, commercialization, and consulting. The company has a wide range of services and products that cater to the needs of their clients. They have a team of experienced professionals that work together to provide the best possible service. The company is committed to providing the highest quality of care to their clients and patients. They have a wide range of experience in different therapeutic areas, which allows them to provide the best possible care to their patients.

Charles River Laboratories

What people are saying: #Experienced #Dedicated #Successful

Charles River Laboratories is one of the top clinical research organizations in the United States. They offer a variety of services to help pharmaceutical and biotechnology companies develop and commercialize their products. These services include preclinical research, clinical research, and manufacturing support. Charles River Laboratories has a long history of helping companies develop new drugs and therapies. They have a team of experienced scientists and clinicians who are dedicated to helping their clients succeed. They offer a wide range of services, from preclinical research to clinical research to manufacturing support. They have a proven track record of success, and they are a trusted partner for many companies. If you're looking for a top clinical research organization to help you develop and commercialize your products, Charles River Laboratories is a great choice.

What people are saying: #Transparent #Innovative #Unique

Caidya is a leading clinical research organization that provides full-service support and vast therapeutic expertise to its clients. The company has a personalized approach to clinical research and offers a unique combination of global experience and knowledge sharing. Caidya's clinical research services are designed to connect you with unrivaled access to specialist knowledge and resources. The company's cutting-edge clinical technology integrates effortlessly to create an ecosystem that meets the specific needs of your study. Caidya's Clarity platform synthesizes data from different systems to create a near real-time view of your trial. This holistic view allows integrated teams within Caidya to transparently share information and data, generating insights to inform your decisions.

What people are saying: #Healthy #Helpful #Compensated

ICON is a clinical research company that is looking for healthy volunteers to participate in studies. The company has locations in Lenexa, KS and Salt Lake City, UT. Participation in a study includes 1 screening visit, 1 stay of 11 nights (12 days) and 1 follow-up visit. Compensation for participation is up to $6400. ICON is a great opportunity for people who want to make some extra money and help out with medical research.

What people are saying: #Trusted #Innovative #Leading

PPD is one of the top clinical research organizations in the United States. They offer a wide range of services, from drug development to clinical trials. They have a team of experienced professionals who are dedicated to helping their clients succeed.

CTI Clinical Trial and Consulting

What people are saying: #Experienced #FullService #Comprehensive

CTI Clinical Trial and Consulting is a full-service CRO that specializes in clinical research and consulting services. They offer a wide range of services including regulatory development, clinical project management, clinical monitoring, biometrics, quality assurance, and real world evidence. They also have a research center where you can participate in clinical trials. The range of services offered by CTI Clinical Trial and Consulting is excellent. They seem to be a one-stop shop for all your clinical research needs. We also like that they have a research center where you can participate in clinical trials. This is a great way to get involved in the latest medical research and to potentially help develop new treatments for various diseases.

Advanced Clinical

What people are saying: #Comprehensive #CustomerFocused #AwardWinning

Advanced Clinical is a top-tier contract research organization that has provided clinical research services to the pharmaceutical and biotech industry for many years. Their global reach and comprehensive solutions make them a perfect partner for companies launching clinical trials. Their focus on satisfaction and customer service is evident in their high employee retention rate and repeat business rate. Their award-winning culture and commitment to excellence make them a great choice for anyone looking for a clinical research partner.

Clinical Research Organizations: What should you be looking for?

The website's mission is to provide accurate, timely, and reliable rankings of clinical research organizations. We aim to provide users with a comprehensive and up-to-date list of the top clinical research organizations so they can make informed decisions about which ones to use. We also provide detailed descriptions of each organization so users can learn more about their work.

Are Clinical Research Organizations (CRO) worth it?

Yes, it is worth hiring clinical research organizations. Here are three reasons why: 1. Clinical research organizations have the experience and expertise to conduct clinical trials effectively. They know how to design trials that meet regulatory requirements, recruit patients, and collect data. 2. Clinical research organizations can help you save time and money. They can manage all aspects of the clinical trial process, so you can focus on other aspects of your business. 3. Clinical research organizations can provide valuable insights into the clinical trial process. They can help you understand the data, identify potential problems, and make decisions about the best course of action.

What to look for when hiring Clinical Research Organizations (CROs)?

Using a Clinical Research Organizations can be a great way to get the medical care that you need. However, there are a lot of questions that you may have about using one. That is why we have provided FAQs for customers interested in using a Clinical Research Organizations. We want to make sure that you have all the information that you need so that you can make the best decision for your medical care.

What are the specific research needs of your organization?

The first step in finding the right Clinical Research Organization (CRO) for your needs is to identify the specific research needs of your organization. These needs will vary depending on the type of research you are conducting, the size and scope of your project, and your budget. Once you have a clear understanding of your research needs, you can begin to research different CROs and compare their services. When considering a CRO, it is important to look at their experience in conducting the type of research you need. Make sure to ask about their success rates and customer satisfaction levels. You should also inquire about their pricing structures and what type of services are included in their fees. It is also important to consider the size of the CRO and their ability to handle your project. Make sure they have the staff and resources necessary to complete your project on time and within budget. Finally, you should also consider the location of the CRO. If your project requires frequent travel, you may want to choose a CRO that is located near your site. If you are conducting research that requires special expertise, you may want to choose a CRO that is located near a research university or hospital.

What is the size and scope of your organization?

Next, you need to understand the size and scope of your organization, and thereby understand the size and scope of the CRO you need to hire. Is the CRO a large, full-service clinical research organization that offers a wide range of services to its clients? Does the CRO have a global reach and is it able to provide its services to clients in a number of different countries? Does the CRO have a large team of experienced and qualified staff who are able to provide a high level of service to its clients? Is the CRO accredited by a number of different bodies and is it able to offer its services to a wide range of clients?

What are the your clinical research priorities?

Finally, you need to understand your organization's clinical research priorities. Are they to develop new treatments for diseases and conditions, to improve the safety and efficacy of existing treatments, or to increase our understanding of the underlying causes of disease? This will help you select a CRO that aligns with your needs.

Key Takeaways about Clinical Research Organizations

When choosing a clinical research organization, it is important to consider the size of the organization, its focus, its location, and its resources. The best clinical research organizations are those that are able to provide the most comprehensive services and the most experienced staff. They should also be able to offer the latest technology and facilities. Top Clinical Research Organizations is dedicated to providing objective rankings of clinical research organizations. We believe that our rankings will help you choose the best organization for your needs. We are committed to providing the most accurate and up-to-date information possible.

Frequently Asked Questions

What is a clinical research organization (cro).

A clinical research organization (CRO) is a company that provides services to pharmaceutical and biotechnology companies to help them outsource and conduct clinical trials. A CRO manages all aspects of a clinical trial, from start to finish, and works with a variety of stakeholders, including investigators, research sites, and patients.

CROs are an important part of the drug development process, as they provide expertise and resources that allow companies to efficiently and effectively conduct clinical trials. Without CROs, many new drugs and treatments would not be possible.

What services do CROs provide?

CROs provide a variety of services to support clinical research, including study design, data management and analysis, regulatory affairs support, and clinical trial management. CROs also provide a variety of other services, such as market research, project management, and training.

What are the benefits of working with a CRO?

There are many benefits of working with a clinical research organization (CRO). CROs can provide expertise and resources that Sponsors may not have internally, and can therefore help to increase the efficiency and quality of clinical trials. In addition, working with a CRO can help to reduce costs associated with clinical trials. CROs also have experience working with a variety of different Sponsors, and can therefore provide valuable insights and perspectives.

What are the risks of working with a CRO?

The risks of working with a CRO include the potential for conflicts of interest, the potential for data manipulation, and the potential for data fraud.

How do CROs ensure the safety of trial participants?

There are a number of ways that clinical research organizations (CROs) ensure the safety of trial participants.

First, CROs typically have staff members who are responsible for monitoring the safety of participants throughout the course of a study. These staff members may be nurses, doctors, or other health care professionals. They typically have experience in managing clinical trials and are familiar with the potential risks and side effects of the drugs or treatments being studied.

Second, CROs typically have established procedures for reporting and managing adverse events. These procedures ensure that any potential safety concerns are promptly identified and addressed.

Third, CROs typically work closely with the sponsor of a clinical trial (usually a pharmaceutical company) to ensure that the sponsor is aware of any safety concerns that arise during the course of the trial. The sponsor is ultimately responsible for the safety of the participants, and the CRO ensures that the sponsor is kept informed of any safety issues that arise.

Fourth, CROs typically conduct regular audits of their clinical trials to ensure that they are being conducted in accordance with good clinical practices and that the rights and safety of participants are being protected.

Finally, CROs typically have insurance policies in place that protect participants in case of any unforeseen events that may occur during the course of a trial.

Overall, the procedures and policies that CROs have in place help to ensure the safety of participants in clinical trials.

How do CROs ensure the quality of data collected during a clinical trial?

CROs ensure the quality of data collected during a clinical trial by following Good Clinical Practices (GCPs).

GCPs are a set of international standards that ensure the quality, safety, and integrity of data collected during a clinical trial. All CROs must adhere to these standards in order to conduct clinical trials.

What happens if a CRO is unable to meet its contractual obligations?

If a CRO is unable to meet its contractual obligations, it may be required to pay damages to the sponsor. The sponsor may also be able to terminate the contract and seek a new CRO.

What is the role of the sponsor in a clinical trial?

What are the responsibilities of the principal investigator in a clinical trial.

The principal investigator (PI) is responsible for the overall conduct of the clinical trial. This includes ensuring that the trial is conducted in accordance with the protocol, applicable regulations, and standard operating procedures. The PI is also responsible for the safety of the trial participants and for ensuring that the data collected are of high quality.

The PI works with the sponsor, other investigators, and the research team to ensure that the clinical trial is carried out correctly and that the data collected are of high quality. The PI is also responsible for the safety of the trial participants.

How are clinical trial sites selected?

When selecting a clinical trial site, sponsors and contract research organizations (CROs) consider a number of factors.

The most important factor is usually the site’s experience and success in conducting similar trials.

Other important factors can include the site’s patient population, geographic location, and facilities.

How are clinical trial subjects recruited?

There are a number of ways that clinical trial subjects can be recruited. One common method is through advertisements in newspapers or other media outlets. Another common method is through word-of-mouth, where people who know about the clinical trial spread the word to others who might be interested. Additionally, clinical trial subjects can be recruited through doctors or other medical professionals, as well as through patient advocacy groups.

How is informed consent obtained from clinical trial subjects?

Informed consent is obtained from clinical trial subjects by providing them with information about the trial in a way that is easy for them to understand. This includes information about the purpose of the trial, the procedures that will be used, the risks and benefits of participating, and their right to withdraw from the trial at any time. Informed consent is not simply a form that subjects must sign; it is a process of communication between the researcher and the subject that should ensure that the subject understands the trial and is willing to participate.

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Top 15 Clinical Research Companies: Leaders in Medical Innovation

What’s on this page:

In the healthcare industry, the number of contract research organizations in the US has reached 2,823 in 2023. This marks a subtle but significant increase of 0.9% compared to the previous year.

This increase signals a vital trend: the growing complexity of finding the best clinical research companies in a crowded field. These organizations aren’t just businesses; they’re important in advancing medicine and developing drugs and therapies.

With such an important task, choosing the right company becomes essential. In this guide, we’ve looked closely at many companies along with their strengths and weaknesses and made a list of the top clinical research organizations. 

By the end, you’ll know which company is the best fit for your needs.

Quick List of Top 15 Clinical Research Companies

Here is a quick overview of the best companies of clinical research:

• IQVIA: Best for data-driven insights and advanced analytics in healthcare research.
• ICON: Best for comprehensive clinical development services and therapeutic expertise.
• Parexel: Best for global biopharmaceutical services, emphasizing regulatory and clinical trial excellence.
• Syneos Health: Best for integrated biopharmaceutical solutions and clinical-commercial capabilities.
• PPD: Best for drug development services with innovative, technology-enhanced trial strategies.
• Labcorp: Best for comprehensive clinical testing and diagnostics services with global reach.
• Medpace: Best for expertise in clinical research and regulatory affairs for pharmaceutical companies.
• Charles River Laboratories: Best for preclinical research and development services, including animal testing and research models.
• PRA Health Sciences: Best for clinical trial expertise and integrated solutions for biopharmaceutical development.
• AdvanCell: Best for innovative cell and tissue-based research solutions for life science industries.
• Dynata: Best for data-driven insights and market research services for informed decision-making.
• Covance: Best for end-to-end drug development solutions, from preclinical to post-marketing.
• MedNet: Best for technology solutions and eClinical platforms for streamlined clinical trials.
• Fisher Clinical Services Inc: Best for global logistics and supply chain services for clinical trial materials.
• Worldwide Clinical Trials: Best for specialized CRO offering personalized clinical research solutions.

3 Best Clinical Research Organizations: Comparison Chart

Here’s a comparison table to highlight the key features and differences among the best companies of clinical research. This table aims to provide a quick overview of each company’s unique strengths and areas of expertise in the pharmaceutical and healthcare research sector.

3 Top Clinical Research Organization List For Advanced Medical Discoveries

Now, we’ll explore the top clinical research organizations (CROs) dedicated to advancing medical discoveries. Let’s jump into the details of these exceptional organizations.

IQVIA is a global leader in clinical research and healthcare data analytics. They play a crucial role in the medical field by providing comprehensive data, advanced analytics, and expert insights. This helps pharmaceutical and healthcare companies make smarter, more effective decisions. 

Why is IQVIA among the best? Their strength lies in their vast database and advanced technology, which enable them to analyze complex healthcare data efficiently. This leads to a better understanding of diseases, more effective treatments, and faster drug development. 

IQVIA’s work is essential because it speeds up the process of bringing new medicines to the market, ultimately benefiting patients worldwide. In short, IQVIA is a key catalyst in advancing global healthcare.

About IQVIA

• Founding Team: Dennis Gillings
• Founding Year: 1982
• Company Size:   86,000

Features of IQVIA

IQVIA, a prominent player in the life sciences sector, is dedicated to advancing healthcare through connected intelligence. Here are some key features of IQVIA in the world of clinical research:

Innovative Clinical Development

IQVIA is reimagining clinical development by intelligently connecting data, technology, and analytics. This approach leads to faster decision-making and reduced risk, enabling the delivery of life-changing therapies more quickly.

Efficient Payment Systems for Clinical Trials 

They have simplified the process of paying sites involved in clinical trials. IQVIA offers the capability to make payments within 30 days, even in challenging locations. This significantly reduces the administrative burden of managing clinical trial payments by up to 90%.

Decentralized Trials Expertise

The company has conducted over 500 studies in more than 75 countries, covering over 30 indications using decentralized trial methodologies. This demonstrates their capability in managing complex, multinational clinical trials.

Global Reach and Impact

With a presence in various regions, including Australia, New Zealand, the Middle East, and Africa, IQVIA’s global footprint allows it to drive healthcare innovations worldwide.

AI and Technology Integration

The company is at the forefront of integrating AI and other technologies in healthcare. Their Healthcare-grade AI promises precision, speed, scale, trust, and reliability, essential for advancing health and improving patient outcomes.

• Extensive, reliable healthcare data enhances market research quality.
• Utilizes AI and machine learning for advanced healthcare insights.
• Specialized focus yields a deep understanding of healthcare dynamics.
• Broad international presence enables diverse and large-scale studies.
• Offers advanced tools for insightful healthcare data analysis.
• Advanced tools can be challenging to use without training.
• Handling sensitive health data raises privacy and security issues.

Our Review of IQVIA

IQVIA, a prominent player in the healthcare and life sciences industry, presents a mixed bag of strengths and weaknesses. On the positive side, we appreciate IQVIA’s extensive expertise in data analytics and healthcare consulting. 

Their comprehensive research and analysis have undoubtedly driven valuable insights and innovations in the sector. Moreover, their global presence allows for diverse perspectives and access to critical healthcare data.

However, we must also acknowledge some shortcomings. IQVIA’s services can be prohibitively expensive for smaller organizations, limiting accessibility. Additionally, the sheer volume of data can sometimes lead to information overload, making it challenging to extract actionable insights.

ICON is a prominent company in the field of clinical research, playing a significant role in advancing medical science. They specialize in designing and conducting clinical trials for new medicines and treatments. 

The work of ICON is crucial because they help determine the safety and effectiveness of these potential medical breakthroughs. They are considered one of the best in clinical research due to their high standards of accuracy, reliability, and ethical practices. 

ICON’s expertise ensures that the clinical trials they manage are conducted efficiently and effectively, leading to faster approval of new treatments. This directly impacts patient care, as it allows quicker access to new, potentially life-saving medicines. 

In essence, ICON’s contribution is vital in driving forward medical innovations.

• Founding Team: John Climax and Ronan Lambe
• Founding Year: 1990
• Company Size: 41,160

Features of ICON

Here are some of the key features of ICON in clinical research:

Diverse Clinical and Scientific Operations

ICON offers a wide range of clinical and scientific operations services, ensuring comprehensive support for various aspects of clinical trials. This includes everything from study design to execution and data analysis.

Decentralized Clinical Trial Solutions

They provide end-to-end services, operational models, and technology to deliver customized solutions for decentralized clinical trials. This approach is increasingly important in today’s clinical research landscape, offering flexibility and efficiency.

Specialized Therapeutic Areas

ICON has expertise across multiple therapeutic areas including cardiovascular, central nervous system, endocrine & metabolic disorders, infectious diseases, internal medicine & immunology, oncology, and more. This broad expertise allows them to handle a wide range of clinical research projects.

Innovative Solutions for Biotech

ICON provides full-service outsourcing and flexible support customized to the specific needs of biotech companies. This includes due diligence and asset valuation, which are critical for biotech firms navigating the complex landscape of drug development.

Advanced Medical Imaging Solutions

Their expert medical imaging solutions support all stages of clinical research, improving decision-making, increasing efficiency, and reducing trial costs.

• Decades of expertise ensure high-quality clinical research.
• Offers wide-reaching capabilities for multi-regional clinical studies.
• Deep understanding of global regulations enhances compliance and efficiency.
• Invests in new technologies for more efficient trial processes.
• Broad range of specialties contributes to comprehensive service offerings.
• Managing multi-regional trials can lead to logistical challenges.
• Rapid growth may strain resources and affect service quality.

Our Review of ICON

When we researched ICON, we found both commendable aspects and areas for improvement. On the positive side, we appreciate their commitment to clinical research and their global presence, which allows for diverse study options. Their experienced team and advanced technology contribute to reliable data collection and analysis.

However, there are some drawbacks to consider. We have noticed occasional delays in project timelines, which can be frustrating. Additionally, the cost of their services tends to be on the higher side, making it a potential barrier for smaller research endeavors.

Parexel is a globally recognized company in clinical research, known for its important role in developing new medical treatments. They are one of the biggest clinical research organizations. Parexel conducts clinical trials, crucial steps in testing the safety and effectiveness of new drugs. 

The work of Parexel is essential because it bridges the gap between medical research and the availability of new treatments to patients. One of the reasons they stand out as one of the best in this field is their rigorous approach to research. 

Their commitment to quality and their global network also enables diverse and large-scale studies, setting them apart from others in the field. These strengths allow Parexel to deliver reliable and valuable data, accelerating the process of bringing new, effective medicines to the market. 

Simply put, Parexel is a key player in transforming medical research into real-world health solutions.

About Parexel

• Founding Team: Josef von Rickenbach and Anne B. Sayigh
• Company Size: 18,900

Features of Parexel

Parexel, a global biopharmaceutical services organization, offers a range of features in clinical research. Here are some key aspects of their approach:

Patient-Centric Approach

Parexel emphasizes a patient-first strategy in their clinical trials. This approach results in deeper and more relevant insights for trial design and execution. This ensures that the trials are more aligned with patient needs and experiences.

Innovative Trial Designs

Parexel employs innovative trial designs to optimize trials for maximum impact. This includes advanced modeling and simulation to predict drug effects ahead of time, which can save time, money, and resources.

Regulatory Compliance and Market Access

Parexel designs studies and endpoints with market access in mind, ensuring that they satisfy global regulations. This approach helps in getting treatments to patients safely and quickly.

Patient Advocacy and Engagement

The company includes patient advocates in their council, using their experiences to improve trial designs. This inclusion demonstrates their commitment to understanding and incorporating patient perspectives in clinical research.

Focus on Speed and Precision

Parexel aims to design neuroscience trials with speed and precision, utilizing the right experts and specializations. This focus is crucial in delivering effective treatments on time.

• Provides advanced technology and analytics for efficient data management.
• Extensive network provides global insights with regional knowledge.
• Expertise in navigating complex regulatory environments worldwide.
• Broad experience across various therapeutic areas ensures versatile solutions.
• Focuses on patient engagement for more effective trial outcomes.
• Rapid expansion can lead to challenges in resource management.
• Concentration in specific areas could pose risks in market shifts.

Our Review of Parexel

Parexel is a notable player in the field of clinical research and pharmaceutical services. We’ve thoroughly analyzed their offerings and found both strengths and areas that need improvement.

On the positive side, Parexel excels in its commitment to innovation and technology. We appreciate their continuous efforts to simplify clinical trials and drug development processes, making them more efficient.

However, we also noticed some downsides. Communication with clients could be more transparent, with clearer updates on project progress. Additionally, there’s room for improvement in terms of ensuring consistency in service quality across different projects.

Other 12 Companies of Clinical Research

In the world of clinical research, beyond the well-known names, there are 12 other companies making significant contributions. Let’s explore their vital role in advancing healthcare.

1. Syneos Health

Syneos Health helps develop medicines by managing clinical trials for new drugs. They’re essential because they ensure medicines are safe and effective. Syneos Health stands out in clinical research for its comprehensive services and global reach, making drug development smoother and faster.

About Syneos Health

• Founding Team: Colin Shannon
• Founding Year: 1980
• Company Size: 28,000

PPD is a group that tests new drugs to see if they’re good and safe. This is crucial for getting new treatments to people. They stand out for their thorough research and global reach.

• Founding Team: Fred Eshelman 
• Founding Year: 1985
• Company Size: 40,000+3

Labcorp does important tests and research for health. They’re needed because they help find out if new treatments are good. They’re among the best for their big labs and fast results.

About Labcorp

• Founding Team: Matthew Benger
• Founding Year: 1978
• Company Size: 75,5000

Medpace focuses on making sure new health treatments are safe. This is key for better medicine. They’re a top choice because of their focus on quality and detail in research.

About Medpace

• Founding Team: August Troendle
• Founding Year: 1992
• Company Size: 5,400

5. Charles River Laboratories

Charles River Laboratories tests drugs and does research to help pets and people stay healthy. They’re essential for safe, new treatments. Their expertise makes them a leader in the field.

About Charles River Laboratories

• Founding Team: Henry Foster
• Founding Year: 1947
• Company Size: 21,400

6. PRA Health Science

PRA Health Science works on finding out if new medicines are safe. This helps everyone get better treatments. They’re known for their excellent research and care in studies.

About PRA Health Science

• Founding Year: 1976
• Company Size: 17,000+

7. AdvanCell

AdvanCell specializes in new treatments, checking if they’re safe and working. Their work is vital for progress in medicine. They’re recognized for their innovation in research.

About AdvanCell

• Founding Team: Andrew Adamovich

Dynata gathers data for health studies. They’re needed for understanding what works in healthcare. They’re a top name for their accurate and wide-reaching data collection.

About Dynata

• Founding Team: Mike Petrullo
• Founding Year: 1940
• Company Size: 5000-10000

Covance helps with drug tests and research to fight diseases. Their role is key for new treatments. They’re celebrated for their comprehensive services and global impact.

About Covance

• Founding Team: Fred Cummings
• Founding Year: 1981
• Company Size: 50,000

MedNet provides software for managing clinical trials. This helps in making research easier and faster. They’re among the best for their tech solutions in research.

About MedNet

• Founding Team: John “Rob” Robertson
• Founding Year: 1996
• Company Size: 51-200

11. Fisher Clinical Services Inc.

Fisher Clinical Services Inc. manages the logistics of clinical trials, ensuring that treatments are tested efficiently. Their work is crucial for the progress of medicine, and they are renowned for their reliability and global network.

About Fisher Clinical Services Inc.

• Founding Team: John Pickering
• Founding Year: 1989

12. Worldwide Clinical Trials

Worldwide Clinical Trials conducts essential research to evaluate new medical treatments. Their work is critical for advancing healthcare. They are distinguished by their global expertise and commitment to innovation in clinical research.

About Worldwide Clinical Trials

• Founding Team: Neal Cutler
• Founding Year: 1986
• Company Size: 3,147

What To Consider When Choosing the Best Clinical Research Companies?

Choosing the right clinical research company (CRC) is crucial for the success of any clinical trial. Here’s a detailed guide on what to consider:

Expertise and Specialization

Always ensure the CRC has expertise in your specific therapeutic area. Companies with experience in similar drug trials or medical devices can better navigate the complexities of your project.

Regulatory Compliance

The CRC must adhere to regulatory guidelines like FDA (US) , EMA (Europe), and others. Check their track record in meeting these standards to avoid compliance issues.

Reputation and Track Record

You should research the company’s history. Look for testimonials, case studies, and reviews from past clients. A company with a strong reputation is likely to deliver quality results.

Project Management Capabilities

Effective project management is key. Assess their ability to manage timelines, budgets, and communication. A CRC that provides transparent, regular updates is preferable.

Patient Recruitment Strategies

Patient recruitment can be challenging. Evaluate their strategies for participant recruitment and retention. Consider their demographic reach and methods for ensuring a diverse participant pool.

Data Management and Analysis

The CRC should have strong systems for data collection, management, and analysis. Ask about their use of Electronic Data Capture (EDC) systems and how they handle data security and confidentiality.

Cost and Financial Terms

Get a clear understanding of the cost structure. Consider the value for money rather than just the lowest cost. Ensure there are no hidden fees and clarify what is included in the quoted price.

How Heartbeat AI Can Help You Get the Best List of Clinical Research Organizations?

Heartbeat AI, with its advanced features, can significantly assist in identifying the best list of clinical research organizations (CROs). Here’s how its various features contribute to this process:

Data Analysis and Processing

Heartbeat AI excels in analyzing vast amounts of data. When it comes to selecting CROs, it can process and analyze information from numerous sources, including past performance records, clinical trial reports, and regulatory compliance data. This thorough analysis helps in identifying CROs with a proven track record of success and reliability.

Machine Learning Algorithms

These algorithms enable Heartbeat AI to learn from historical data and improve its recommendations over time. By understanding trends and patterns in the successful execution of clinical trials, it can better predict which CROs are likely to meet your specific needs.

Predictive Analytics

Heartbeat AI uses predictive models to forecast future trends and outcomes based on historical data. This can be invaluable in predicting the success rate of CROs in upcoming projects, thus aiding in making more informed choices.

Customization and Personalization

The AI can be customized to your specific requirements. If you’re focusing on a specific therapeutic area or clinical trial phase, Heartbeat AI can prioritize specialized CROs in these fields.

Real-time Data Updates

The healthcare and pharmaceutical landscapes are constantly changing. Heartbeat AI’s ability to integrate and analyze real-time data ensures that the recommendations are based on the most current information available.

Integration with External Databases

Heartbeat AI can integrate with various external databases and platforms. This enables it to pull in comprehensive information about CROs from diverse sources, enhancing the accuracy of its recommendations.

Claim $500 of Free Data  

Summing up, we’ve explored the best clinical research companies, diving into their features, strengths, weaknesses, and more. Clinical research is vital in healthcare; it’s key for advancing medical knowledge and developing new treatments. 

With this guide, you’re equipped to find the right clinical research company that meets your specific needs. Whether it’s for innovative therapies, drug development, or medical advancements, choosing the right partner is crucial. This guide serves as a valuable resource to help you make an informed decision in the complex world of clinical research.

Frequently Asked Question

What services do companies of clinical research offer.

Clinical research organizations offer a wide range of services, including protocol development, patient recruitment, data collection and analysis, regulatory compliance, and more.

What is the role of a clinical research coordinator?

A clinical research coordinator is responsible for managing various aspects of a clinical trial, including patient recruitment, data collection, and ensuring compliance with protocols.

What is informed consent in clinical research?

Informed consent is the process by which participants in a clinical trial are fully informed about the study’s purpose, risks, and benefits. They voluntarily agree to participate based on this information.

Top Clinical Research Organisations (CRO) 2022

• Author Company: PharmiWeb.Jobs
• Author Name: Lucy Walters
• Author Email: [email protected]
• Author Website: https://www.pharmiweb.jobs/

In this article, we’ve rounded up some of the top Clinical Research Organisations (CROs) across the globe…

Headquartered in North Carolina, U.S., IQVIA is a leading global provider of clinical research services to the life sciences industry. With over 74,000 employees, IQVIA has been recognised as one of Fortune’s ‘World’s Most Admired Companies’ (2021), Flex Jobs’ ‘Top 100 Remote Work Companies to Watch’ (2021) and Forbes’ ‘World’s Best Employers’ (2020).

Browse current jobs with IQVIA here .

Also headquartered in North Carolina, U.S., Labcorp (formerly Covance) is a leading global life sciences company working to provide vital information to help doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions. Established in 1986, Labcorp’s Clinical Research Unit in Leeds, U.K., is where the organisation carries out clinical trials for some of the world’s leading pharmaceutical and biotechnology companies.

Browse current jobs with Labcorp here .

Syneos Health

Syneos Health is the only full-service biopharmaceutical solutions company in the world, bringing together the best clinical and commercial minds to improve patient access to medicine. With headquarters in North Carolina, U.S.,  Syneos Health has been recognised across the globe for its fit-for-purpose CRO solutions. The organisation has been awarded ‘Top CRO to Work With’ among top 10 global CROs in 2013, 2015 and 2017, and were the winner of the 2017 Society for Clinical Research Sites Eagle Award.

Browse current jobs with Syneos Health here .

ICON is a global, leading clinical research organisation providing services to pharmaceutical, biotechnology, medical device and government and public health organisations. ICON specialises in the planning, management, execution and analysis of Phase 2-3 clinical trials, with functional and therapeutic expertise including cardio-metabolic, oncology/hematology, infectious diseases, neurology/psychiatry, rare disease and more.

Browse current jobs with ICON Clinical Research here .

Headquartered in Massachusetts, U.S., Parexel is one of the largest clinical research organisations, providing services that help life science and biopharmaceutical organisations transform scientific discoveries into new treatments. With global study locations in Baltimore, Los Angeles, Berlin and London, Parexel offers comprehensive clinical development services from First-in-Human through Phase IV and post-marketing. They were named ‘Best Contract Research Organization’ in December 2020 and ‘Top CRO to Work With’ in 2022.

Browse current jobs with Parexel here .

Charles River Laboratories

Charles River is a leading provider of drug discovery services to the bioscience community, collaborating on projects from small, single discipline projects to fully integrated drug discovery projects. With more than 18,400 employees worldwide, Charles River currently operates in 100+ facilities in more than 20 countries and has supported the development of more than 80% of the drugs approved by the FDA for the past 3 years.

Browse current jobs with Charles River Laboratories here .

Medpace is a global, full-service clinical contract research organisation providing clinical development services (Phase I-IV) to the biotechnology, pharmaceutical and medical device industries. With headquarters in Ohio, U.S., Medpace has coverage across six continents and is the only global CRO to have a fully integrated Clinical Research Campus, with subsidiaries including central laboratories, a clinical pharmacology unit, a bioanalytical laboratory and other core laboratories.

Worldwide Clinical Trials

Worldwide Clinical Trials is a global, mid-sized, CRO that provides top-performing, preclinical, and Phase I-IV clinical development services to the biotechnology and pharmaceutical industries. The organisation has been recognised for excellence and honoured in five categories in the 2022 CRO Leadership Awards, marking the ninth consecutive year that Worldwide has been recognised as a high-performing CRO based on direct survey feedback from pharmaceutical and biotech professionals.

Browse current jobs with Worldwide Clinical Trials here .

Find more of the industry's top Clinical Research organisations currently advertising on PharmiWeb.Jobs here . 

View the top CROs in 2023 here. 

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Top 10 Global Clinical Research Organizations in 2021

In 2020, a global outbreak of the new crown epidemic disrupted the business activities of almost all companies, and the drug R&D and production of pharmaceutical companies was no exception. As a CRO/CDMO company serving pharmaceutical companies, its market share and global ranking have also changed when the global market order is chaotic.

　　 2021 Global CRO Ranking TOP10

Note: ①This list covers CRO in a broad sense, and its business areas cover pre-clinical research, clinical trials, pharmaceutical development, and commissioned production of raw materials and drugs (CDMO and CMO) related to new drug research and development; ②The two data of ICON+PRA are directly related Plus; ③Lonza’s income is 4.5 billion Swiss francs, and the exchange rate is converted to US dollars at 1.1; ④Catalent’s fiscal year is July 2019 to June 2020; ⑤Wuxi includes Wuxi AppTec and WuXi Biologics, and the combined income is converted to US dollars at an exchange rate of 6.8; ⑥Parexel has been delisted after being acquired by a consortium in 2017. Only the income announced in 2018 is here for reference.

Medicilon is a professional pharmaceutical preclinical integrated R&D service contract research organization (CRO), providing a full range of one-stop new drug R&D services, in compliance with Chinese and international filing standards, to pharmaceutical companies and research institutions around the world. Our services cover the entire process of preclinical new drug research, including drug discovery, pharmacology research and preclinical research. Our drug discovery services include chemical synthesis, compound activity screening and optimization, structural biology research, protein target validation, etc.; Pharmacological researches include process research of API and formulation, quality standards and stability research, etc.; Preclinical researches include pharmacodynamics, pharmacokinetics, toxicological safety evaluation, etc.

　　 Judging from the TOP10 list, the top two CRO companies in the world both have revenues of more than 10 billion U.S. dollars, which is a huge gap with the players behind them, and the dominant position is unbreakable. ICON’s acquisition of PRA has become a major event in the industry, which has greatly improved the ranking of the new company’s business scale, making it the third largest in the world in one fell swoop.

　　 Syneos is the only company on the list that has shrunk in performance (Parexel is not known), while WuXi is the only Chinese element on the list. Its growth rate is far ahead, and its ranking is steadily rising. Mainly because under the new crown virus epidemic, China was the first to restore order to resume work and production, and a large number of orders were transferred to China. Charles River, which once gave up the acquisition of WuXi, has now been surpassed by WuXi.

　　 Labcorp and Catalent have also benefited from the COVID-19 pandemic, including the testing business and the vaccine production business, respectively. Companies with a larger proportion of clinical research businesses are more affected by the pandemic, but generally recover in the fourth quarter of 2020.

　　 This article gives a brief introduction to the world’s TOP10 CRO companies.

　　NO.1 LabCorp

The main business of LabCorp is clinical diagnostics. After successive acquisitions of Covance and Chiltern, it has entered the field of drug research and development, whether it is preclinical research or clinical research. One of the global leaders. After these two big mergers and acquisitions, the company has become the world’s largest CRO.

　　 In 2020, the company’s revenue is approaching US$14 billion, an increase of 21% over the previous year. Affected by the new crown virus epidemic, most industries and companies around the world are facing varying degrees of impact, but it is very good for the company’s diagnostic business. The new crown virus testing business contributed as much as 24.1% to the 2020 annual performance.

　　The company has a large and complete laboratory system not only in North America, but also in the world. In 2020, the total number of global employees will reach 75,000.

　　NO.2 IQVIA (Ai Kunwei)

　　 Although IQVIA is slightly lower than Labcorp in terms of performance and size, the industry generally believes that IQVIA’s influence is greater than Labcorp, which means I have to mention the company’s predecessor.

　　 In 2016, Quintiles and IMS Health merged to form IQVIA, which became the most important event in the industry that year. These two companies are the leaders and the gold standard in their respective subdivisions. Such a strong combination will inevitably lead to a giant, but because Labcorp has entered the field of drug research and development in about the same time, it has to be resigned. However, in the subdivision field, each has its own unique advantages.

　　 In 2020, the company’s revenue was 11.36 billion U.S. dollars, an increase of only 2.% compared with the previous year. The main reason is that clinical research is affected by the new crown virus and the progress is slow, especially in North America. Fortunately, in the fourth quarter, various businesses have clearly recovered, and it can be predicted that the growth in 2021 will be better than that in 2020.

　　 In 2020, IQVIA will have 70,000 employees worldwide.

　　NO.3 ICON+PRA

　　PRA’s revenue in 2020 was US$3.183 billion, an increase of 3.8% over the previous year; while ICON’s revenue in 2020 was US$2.797 billion, a decrease of 0.3% over the previous year. The two companies have 19,000 and 16,000 employees respectively.

　　 In February 2021, ICON announced the acquisition of PRA for US$12 billion. The new company will achieve growth of more than 10% in the first year, and will grow by more than 20% in the future.

　　 These two were originally in the global TOP10. Relatively speaking, ICON is slightly smaller than PRA, but this does not prevent ICON from acquiring PRA in a way that small fish eat big fish. After the merger, the new company came to the third place in the world in one fell swoop.

　　NO.4 Lonza (Lonza)

　　Lonza is undisputedly the world’s largest CDMO company.

　　 The Lonza Group operates two major businesses, of which the Lonza Special Ingredients business (LSI) focuses on the microbial control of personal care products, and the volume within the group is relatively small. The pharmaceutical and biotechnology and nutrition business (LPBN) is Lonza’s main source of income, covering from early discovery, customized development to the production of active pharmaceutical ingredients and innovative dosage forms, and is a well-known CDMO business in the industry.

　　 In 2020, the company’s revenue will be 4.5 billion Swiss francs, achieving 12.5% growth. The company also decided to divest the relatively small special component business and make structural adjustments to make the business more focused and improve transparency, productivity and operational efficiency.

　　 In response to the new coronavirus epidemic, Lonza used global production capacity to provide a full range of development and production services for Moderna’s new coronavirus RNA vaccine (mRNA-1273), with an estimated annual production capacity of 1 billion doses.

　　 PPD, founded in 1985 by Fred Eshelman, Ph.D., had its first IPO in 1996. In 2011, the company was privatized with a US$3.9 billion acquisition. It will be listed again on Nasdaq in the United States in 2020.

　　 I have to say that PPD has made great moves in China, including the completion of two mergers and acquisitions in China in 2009, and the acquisition of Igus and Baonuo, which were large in China at that time. Among them, Baonuo founder John V. Oyler founded BeiGene in 2010.

　　 PPD’s 2020 revenue is 4.68 billion U.S. dollars, achieving 16.1% growth.

　　NO.6 Syneos Health

　　 In 2017, INC Research and Inventiv Health merged to form Syneos Health, which once climbed to the third position in the world.

　　 In 2020, the company’s revenue was 4.42 billion U.S. dollars. It is the only company on the list that has suffered negative growth in performance due to the impact of the new crown virus epidemic, and its ranking has also declined.

　　NO.7 WuXi

Although WuXi Biologics and WuXi PharmaTech are two independently-operated listed companies, considering that WuXi Biologics originated from WuXi PharmaTech and the chairman of the two companies is the same person, the two companies are referred to as WuXi PharmaTech. Department of consolidated calculations.

　　 WuXi’s business covers all aspects of new drug research and development, almost all-encompassing and omnipotent, and it is already a global giant. Although it has not yet become the global leader, the influence that everyone feels is undoubtedly insurmountable by its peers.

　　The consolidated revenue of WuXi in 2020 is approximately US$3.26 billion, an increase of 31.4% over 2019. The number of employees reached 32,000. Regardless of income or personnel, the growth rate is far ahead of its peers. And judging from the development trend in recent years, it will still maintain rapid growth.

　　 The negative impact of the new crown virus epidemic on the company is small in scope, mild in severity and short in time. On the contrary, the epidemic has played a major role in promoting performance to some extent. On the one hand, the company has undertaken a number of R&D and production projects related to the new crown virus. On the other hand, the raging overseas epidemic has caused some orders to be transferred to China.

　　NO.8 Catalent

　　 Catalent was established in 2007, and its expertise is in the production and packaging of preparations, including oral, injection and respiratory administration methods. In fact, the company’s history can be traced back to Scherer, which was established in 1933. The company developed a rotary pressing equipment for soft capsules, which also explains Catalent’s global leadership in soft capsule production. In 2014, the company was listed on the New York Stock Exchange.

　　 Catalent’s full fiscal year is different. Most of them are based on the calendar year, while Catalent is from July to June of the following year. For example, the fiscal year 2020 is from July 2019 to June 2020. The company’s operating income for fiscal year 2020 was US$3.094 billion, a year-on-year increase of 22.89%.

　　The new coronavirus vaccine developed by Johnson & Johnson is produced by Catalent.

　　NO.9 Charles River

The company’s business has three main parts: Research Models and Services (RMS), Discovery and Safety Assessment (DSA), and Manufacturing Support. In short, they are animal models, safety evaluation, and production. .

　　The company’s revenue in 2017 was US$2.92 billion, an increase of nearly 11.5% over the previous year. It has approximately 17,000 employees worldwide.

　　 In 2010, Charles River prepared to acquire WuXi AppTec for a total price of US$1.6 billion. Because the plan was opposed by the company’s shareholders, the agreement had to be unilaterally terminated and WuXi AppTec paid 30 million US dollars for the break-up fee. Since then, WuXi AppTec has firmed its own development path and started a drastic expansion plan with this break-up fee. As the so-called “Hedong in ten years, Hexi in ten years”, Charles River has now been surpassed by WuXi. I don’t know how the shareholders who voted against it felt. Just in time for the sentence: “Yesterday you were indifferent to me, but today I let you not be able to climb high.”

　　NO.10 Parexel

　　 In 2017, the British private equity firm Pamplona Capital Management announced the completion of the US$5 billion acquisition of Parexel. Parexel subsequently delisted. Since then, its performance has not been announced. Here we refer to the data released in 2018, which is 2.5 billion US dollars and about 19,000 employees. It stands to reason that both figures have increased in the past three years, but the specifics are unknown.

　　 In 2021, the company decided to divest the information system and medical imaging business, which also includes the clinical trial management system, electronic data acquisition system, and registration management system. The new company, Calyx, has 2,300 employees. As a result, Parexel’s revenue and scale will shrink.

　　 In addition to traditional clinical research, Parexel is characterized by the preparation of registration documents and the ability to communicate with the drug administration department. The reason for this feature is that Jingding has a self-developed registration and declaration management system (eCTD software), and that it has established a strong registration and declaration team, of which more than 100 have been in the mainstream pharmaceutical market. Reviewers who have worked in government departments.

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• Industry Features

Headquartered in North Carolina, U.S., IQVIA is a leading global provider of clinical research services to the life sciences industry. With over 74,000 employees, IQVIA has been recognised as one of Fortune’s ‘World’s Most Admired Companies’ (2021), Flex Jobs’ ‘Top 100 Remote Work Companies to Watch’ (2021) and Forbes’ ‘World’s Best Employers’ (2020).

Browse current jobs with IQVIA  here .

Also headquartered in North Carolina, U.S., Labcorp (formerly Covance) is a leading global life sciences company working to provide vital information to help doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions. Established in 1986, Labcorp’s Clinical Research Unit in Leeds, U.K., is where the organisation carries out clinical trials for some of the world’s leading pharmaceutical and biotechnology companies.

Browse current jobs with Labcorp  here .

Syneos Health

Syneos Health is the only full-service biopharmaceutical solutions company in the world, bringing together the best clinical and commercial minds to improve patient access to medicine. With headquarters in North Carolina, U.S.,  Syneos Health has been recognised across the globe for its fit-for-purpose CRO solutions. The organisation has been awarded ‘Top CRO to Work With’ among top 10 global CROs in 2013, 2015 and 2017, and were the winner of the 2017 Society for Clinical Research Sites Eagle Award.

Browse current jobs with Syneos Health  here .

ICON is a global, leading clinical research organisation providing services to pharmaceutical, biotechnology, medical device and government and public health organisations. ICON specialises in the planning, management, execution and analysis of Phase 2-3 clinical trials, with functional and therapeutic expertise including cardio-metabolic, oncology/hematology, infectious diseases, neurology/psychiatry, rare disease and more.

Browse current jobs with ICON Clinical Research  here .

Headquartered in Massachusetts, U.S., Parexel is one of the largest clinical research organisations, providing services that help life science and biopharmaceutical organisations transform scientific discoveries into new treatments. With global study locations in Baltimore, Los Angeles, Berlin and London, Parexel offers comprehensive clinical development services from First-in-Human through Phase IV and post-marketing. They were named ‘Best Contract Research Organization’ in December 2020 and ‘Top CRO to Work With’ in 2022.

Browse current jobs with Parexel  here .

Charles River Laboratories

Charles River is a leading provider of drug discovery services to the bioscience community, collaborating on projects from small, single discipline projects to fully integrated drug discovery projects. With more than 18,400 employees worldwide, Charles River currently operates in 100+ facilities in more than 20 countries and has supported the development of more than 80% of the drugs approved by the FDA for the past 3 years.

Medpace is a global, full-service clinical contract research organisation providing clinical development services (Phase I-IV) to the biotechnology, pharmaceutical and medical device industries. With headquarters in Ohio, U.S., Medpace has coverage across six continents and is the only global CRO to have a fully integrated Clinical Research Campus, with subsidiaries including central laboratories, a clinical pharmacology unit, a bioanalytical laboratory and other core laboratories.

Browse current jobs with Medpace here.

Worldwide Clinical Trials

Worldwide Clinical Trials is a global, mid-sized, CRO that provides top-performing, preclinical, and Phase I-IV clinical development services to the biotechnology and pharmaceutical industries. The organisation has been recognised for excellence and honoured in five categories in the 2022 CRO Leadership Awards, marking the ninth consecutive year that Worldwide has been recognised as a high-performing CRO based on direct survey feedback from pharmaceutical and biotech professionals.

Browse current jobs with Worldwide Clinical Trials here .

Find more of the industry's top Clinical Research organisations currently advertising on  PharmiWeb.Jobs   here . 

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Sara's only symptom was fatigue. but after some routine tests, she was diagnosed with breast cancer..

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Pharma IQ showcases the top 10 Contract Research Organizations across the Pharma IQ network.

Much of the world’s population is in desperate need of better medical care. This need is a large driving force behind drug discovery’s mission to uncover new medicines.

The drug discovery process is complex and stubborn. The clinical stage, in particular, is resource intensive, demanding and high risk . A fine balance is required to execute this stage correctly.

Clinical Research Organisations (CROs) supporting drug manufacturers on their road to discover and approve drugs of the future by absorbing some of the clinical stage’s the burdens. Some of the activities covered are:

• Data research
• Project management
• Trials that are run post approval
• Pre-clinical

This relationship, which is built on trust and skill, can award manufacturers with heightened expertise as well as cost and time efficiencies.  These benefits come at the cost of duties such as intensive communication management , confidentiality concerns and regulatory considerations.  

The trend towards outsourcing to CROs isn’t expected to fizzle out anytime soon, especially as the spread of clinical trials across the world is growing. The global market is forecasted for strong growth, after reaching US$36.2bn in 2017 it is projected to climb by another US$20bn over the next five years.    

Read more: How to improve the success rates of clinical trials

What to look for in a cro.

Pharmaceutical and biologic firms need to select reliable partners who will add value to their medical research. This is a complex decision process involving the evaluation of many variables.                                                                    

We invited the Pharma IQ community to vote for the leading CROs in the pharmaceutical and the biologic industry according to their own experiences.

Our research base is made up of participants from mainly big pharma or biotech, SME pharma and consultants. Other entities included in this research include government bodies, medical device manufacturers and public hospitals.  

What criteria makes an excellent CRO?

The rising public pressure on medicine prices and spend by pharmaceutical firms, drives the appeal of outsourcing as a way to cool costs.

However, as pharma continues to wrestle with stagnant innovation levels, despite the funding boost to R&D pipelines, cheaper running costs are no longer the primary motive for outsourcing. In fact, this was considered as the last priority for our response base.

Read more: How to automate the data lifecycle to accelerate drug discovery

(respondent’s could vote for more than one answer) .

One respondent noted that on top of having a combination of all the listed attributes, they desired the ‘right’ culture and expertise within the actual group of people proposed for the study. 

Availability in certain regions, emerging markets, for example, and being update to date with recent regulatory changes were highlighted as key factors by some participants.

Just over 55% of our base agreed that quality is the most important differentiator when selecting a CRO .  

Regarding the importance of quality, in association with the Trial Master File ( TMF) and Inspection Readiness event , Ivan Walrath, Head of Audit and Inspection Quality at Pfizer noted how important it is CROs recognized the significance of this file. The TMF is what regulators will consult to evaluate the quality of the science behind the product at hand.

He added: “What I’ve seen when these partnerships have worked well is a good level of communication and integration between the people from the CRO and the sponsor working together to execute a trial.

“When you have a well-functioning team, even across those organizational boundaries, everybody gets behind what needs to happen from a quality standpoint, from a compliance standpoint and other important aspects like hitting timelines.”

Our  2018 study  found that Clinical trial supply has seen a reduction in wastage rates thanks to smarter integration and alignment with enrollment rates.

This improvement was achieved through Interactive Voice Response Systems (IVRS) and Interactive Response Technology (IRT), these tools were one of the top spend priorities.

Read more: Top five countries running the most clinical trials

The majority of the base noted that contract reviews would happen only when an issue came up or on an annual basis.

A few participants clarified that reviews are ongoing as part of their oversight to ensure compliance with contract services, but “not for the purpose of switching CROs, that would only be done in extreme circumstances of failure to perform.”

Ending a partnership with a CRO

Similar to 2017’s results, lack of quality was the aspect voted most likely to end a partnership with a CRO, attracting 65% of the votes.  A high level of mistakes was the next option with 12% of the vote.  One participant proceeded to clarify a legitimate reason being:

“Significant failure to meet obligations of contract, missing multiple milestones, without reasonable cause or appropriate risk mitigation.”

Pharma IQ top 10 CROs

1.       iqvia, 2.       parexel, 3.       syneos health, 4.       covance, 5.       icon, 6.       pra health sciences, 7.       ppd, 8.      chiltern, 9.      fisher clinical services, 10.   medpace, read our updated guide to the 10 biggest cros in the pharma sector for 2022.

Firms that attracted recognition from the network as rising stars include:

·         Charles river laboratories

·         pivotal, ·         psi, ·         pharmolam.

Further comments included: “After 25 years in the business, always with small Biotechs, I have learned that niche CROs provide the best service for our needs (Argint and CONET). I tend to avoid large CROs when at all possible.”

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A Comprehensive Guide to Clinical Research Organizations (CROs)

Clinical Research Organizations (CROs) play a crucial role in the pharmaceutical, biotechnology, and medical device industries. They provide support to companies in the form of research services outsourced on a contract basis. In this comprehensive guide, we will explore what CROs are, who their clients are, the stages of the research process they are typically involved in, and delve into the exciting career opportunities within the field of clinical research.

Table of Contents

Introduction to Clinical Research Organizations (CROs)  The Role of CROs in the Research Process  Services Offered by CROs  Clients and Partners of CROs  Careers in Clinical Research  Clinical Research Associate (CRA) Roles and Responsibilities  Educational and Professional Requirements for Clinical Research  Careers Advancement Opportunities in Clinical Research  Tips for Success in Clinical Research  Careers Resources and Professional Organizations  Conclusion

Introduction to Clinical Research Organizations (CROs)

Clinical Research Organizations (CROs) are companies that provide support to the pharmaceutical, biotechnology, and medical device industries in the form of research services outsourced on a contract basis. They offer a wide range of services , including biopharmaceutical development, clinical development, clinical trials management, and pharmacovigilance. CROs aim to simplify the entry into drug markets and streamline the drug development process by providing specialized expertise and resources.

The Role of CROs in the Research Process

CROs play a crucial role in the research process, from the early stages of drug discovery and development to the final stages of clinical trials and commercialization. They work closely with their clients to design and execute clinical trials, ensuring adherence to regulatory requirements and ethical standards. CROs also provide support in data management, statistical analysis, and the preparation of regulatory submissions.

Services Offered by CROs

CROs offer a wide range of services to their clients, including but not limited to: 

Biopharmaceutical development : CROs assist in the development of new drugs, from preclinical studies to early-phase clinical trials. Clinical development: CROs design and manage clinical trials, ensuring compliance with regulatory requirements and ethical standards. 

Clinical trials management: CROs oversee all aspects of clinical trials, including site selection, patient recruitment, data collection, and safety monitoring. 

Pharmacovigilance : CROs monitor the safety of drugs and medical devices during clinical trials and after they are on the market. 

Real-world evidence and outcomes research : CROs collect and analyze data from real-world sources, such as electronic health records, to generate evidence on the safety and effectiveness of drugs and medical devices. CROs conduct studies to evaluate the effectiveness and safety of drugs and medical devices in real-world settings. 

Clients and Partners of CROs

CROs work with a diverse range of clients, including pharmaceutical  companies,  biotechnology firms, medical device manufacturers, research institutions, and government organizations . They collaborate closely with their clients to ensure that research studies are conducted efficiently, safely, and in compliance with regulatory requirements. CROs also partner with academic institutions and foundations to support their research initiatives.

Careers in Clinical Research

Clinical research offers exciting career opportunities for individuals interested in the scientific, regulatory, and operational aspects of drug development. 

Careers in clinical research span a wide range of roles, including Clinical Research Associate (CRA), Clinical Project Manager, Data Manager, Biostatistician, and Medical Writer, among others. These roles require a combination of scientific knowledge, attention to detail, critical thinking, and strong communication skills.

Clinical Research Associate (CRA) Roles and Responsibilities

Clinical Research Associates (CRAs) play a crucial role in the execution and monitoring of clinical trials. Their responsibilities include site selection and initiation, monitoring study progress, ensuring compliance with protocols and regulatory requirements, and maintaining accurate and complete documentation. CRAs work closely with investigators, study coordinators, and other stakeholders to ensure that trials are conducted safely and efficiently.

Educational and Professional Requirements for Clinical Research Careers

Careers in clinical research typically require a strong educational background in life sciences or a related field. Many positions, such as CRAs, require a bachelor's or master's degree in a scientific discipline. Professional certifications, such as the Certified Clinical Research Associate (CCRA) certification, can enhance career prospects and demonstrate expertise in the field.

Advancement Opportunities in Clinical Research

Clinical research offers ample opportunities for career advancement and professional growth. Experienced professionals can progress to more senior roles, such as Clinical Project Manager or Clinical Operations Director, where they oversee the planning and execution of multiple clinical trials. Continuing education, networking, and staying updated with industry trends are essential for career advancement in clinical research.

Tips for success in seeking a Career in Clinical Research

To succeed in clinical research careers, professionals should continuously develop their scientific knowledge, stay updated with regulatory requirements, and enhance their communication and project management skills. Networking, building relationships with key stakeholders, and seeking mentorship can also contribute to career advancement in the field.

Resources and Professional Organizations for Clinical Research Professionals

Several resources and professional organizations cater to the needs of clinical research professionals. These include industry publications, online forums, conferences, and professional associations. Organizations such as the Association of Clinical Research Professionals (ACRP) and the Society of Clinical Research Associates (SoCRA) provide educational resources, networking opportunities, and professional certifications for clinical research professionals.

Clinical Research Organizations (CROs) play a vital role in the pharmaceutical, biotechnology, and medical device industries by providing research services on a contract basis. They offer a wide range of services to support the development and execution of clinical trials, ensuring compliance with regulatory requirements and ethical standards. 

Careers in clinical research offer exciting opportunities for individuals interested in the scientific, regulatory, and operational aspects of drug development. By partnering with CROs and pursuing careers in clinical research, professionals can contribute to the advancement of medical science and the development of innovative therapies.

If you're interested in exploring careers opportunities in clinical research, view our current vacancies at ICON today.

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What is a Clinical Research Organization?

The four phases of clinical trials.

• Establishes the effect of a new drug in humans
• Usually conducted on small (12-50) populations of healthy volunteers and/or patients
• Determines a drug's toxicity, absorption, distribution, metabolism and excretion
• Tests a drug for safety and efficacy in a relatively small (200-500) population of patients
• Patients are afflicted with the disease or condition for which the drug is being developed
• Tests the drug in relatively large populations of patients (500-5,000 or more)
• Usually compares the new drug to placebo or to the standard therapy currently being used for the disease of interest
• Results usually provide package insert info (Prescribing Information for doctors, and Patient Information materials)
• Conducted after a drug has been approved by a Regulatory Authority
• Compares the drug to competitor drugs, to explore additional patient populations or disease indications, or to further assess the safety of the drug

Key Functions of CROs

CROs serve as an important component of the drug development ecosystem, offering a wide range of services that encompass every phase of the clinical trial process. Some of the key functions of CROs include:

Protocol design and development : CROs assist sponsors in creating robust and scientifically sound study protocols that define the scope, objectives, and methodologies of the clinical trial.

Patient recruitment and retention : CROs employ various strategies to identify and enroll eligible patients for clinical trials, ensuring that participant targets are met. They also focus on patient retention through engagement and support.

Regulatory and ethics compliance : CROs navigate complex regulatory requirements and ensure adherence to ethical considerations, protecting the rights and well-being of study participants.

Clinical trial operation : CROs manage the day-to-day operations of clinical trials, including site selection, monitoring, data collection, and adverse event reporting, among other activities.

Data management and biostatistics : CROs employ advanced technologies and robust data management systems to collect, scrutinize, and analyze trial data, generating high-quality evidence to support regulatory submissions.

Quality assurance and control : CROs implement comprehensive quality assurance measures to ensure that clinical trials are conducted in accordance with Good Clinical Practice (GCP) guidelines, industry standards, and regulatory requirements.

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Clinical Research Employers

Search form, companies working with clinical research also work in 22 other areas:.

• Clinical Trial Services (7)
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• Services (3)
• Artificial Intelligence (2)
• Education (2)
• Biostatistics (1)
• Contract Development (1)
• COVID-19 (1)
• Genomics (1)
• Health Care (1)
• Immunoassays (1)
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• Molecular Diagnostics (1)
• Oncology (1)
• Pharmaceuticals (1)
• Pharmacogenomics (1)
• Regenerative Medicine (1)
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Worldwide Clinical Trials Recognized as Highest Rated Phase I Provider for Overall User Preference in 2024 Industry Standard Research Phase I Benchmarking Report

Primary market research from key clinical development decision makers corroborates CRO’s industry leadership achievements and data

RESEARCH TRIANGLE PARK, N.C. – 25 JUNE 2024 – Worldwide Clinical Trials (Worldwide), a global full-service contract research organization (CRO), proudly announces results of the 2024 Industry Standard Research (ISR) Phase I CRO Benchmarking Report. The findings confirm the importance of CRO partnerships and reinforce Worldwide’s status as a top-performing CRO for Phase I services . View the full report here .

In an industry characterized by market consolidation, other recent surveys highlight increasing concerns among pharmaceutical and biotech firms regarding the stability of large CROs. This environment underscores the need for reliable CRO partners who can deliver foundational Phase I research with consistent high quality. The ISR report not only validates Worldwide’s proven track record as a strong CRO partner but also underscores its steadfast dedication to operational excellence and leadership in an environment in which Phase I clinical trials are increasingly complex with elevated sponsor expectations and timelines.

The ISR Phase I CRO Benchmarking Report is the output of a web-based, quantitative survey of key clinical development outsourcing decision makers from small, midsize, and large biopharma companies, conducted in the fourth quarter of 2023. Worldwide was recognized as a leader with the following key metrics:

• User Preference . Worldwide ranks the highest Phase I service provider among users asked, “Which Service provider would you prefer to work with for Phase I services if the decision were completely up to you?”
• Leadership . Worldwide’s leadership scores for Phase I services outperform all other midsize CROs.
• Staff Characteristics . Worldwide is the highest rated Phase I CRO for therapeutic expertise and holds a joint first position for timely project communications.
• Services . Worldwide ranks No. 2 among the Top 3 CROs for Phase I core services – outperforming all other Phase I providers for biostatistics and data management.
• Real-Time Data Access . Worldwide ties for second position in its use of technology for real-time data access.

“These benchmark metrics are a clear indication of our commitment to continuous improvement and operational excellence at our Bioanalytical Lab and Clinical Pharmacology Unit ,” said Mike Mencer , Executive Vice President and General Manager, Early Phase at Worldwide. “Phase I studies require comprehensive support to ensure both subject safety and scientific integrity. From our medical and scientific consultation and regulatory services to clinical oversight, data management, and pharmacokinetics, it’s gratifying to have further evidence that sponsors value our partnership, leadership, therapeutic expertise, and operational acumen.”

“As a sponsor, my experience working with Worldwide Clinical Trials is consistent with their results in the 2024 ISR Phase I CRO Benchmarking Report,” said Olga Ohayon, Senior Director, Clinical Operations, Rhythm Pharmaceuticals . “Through its full suite of Phase I service offerings, and its technical and therapeutic expertise, Worldwide is a truly valuable CRO partner that is able to flex to our needs and meet our timelines. It’s easy to see why they scored so high in ISR categories like ‘User Preference,’ ‘Leadership,’ and ‘Services.’”

“Sponsors tell me all the time that they like working with Worldwide because we’re as passionate about their study as they are. They want a true partner in their studies, and they feel Worldwide is an extension of their team,” said Worldwide’s CEO Peter Benton . “With the increasing complexity of Phase I trials, we understand the importance of real partnerships. We look forward to continuing to build successful relationships and helping sponsors of all sizes through their Phase I research.”

For its ISR rankings, Worldwide was recently recognized for excellence in nine categories in the 2024 CRO Leadership Awards , presented by Clinical Leader , marking the 11th consecutive year the CRO has been rated as a top-performer. Based on customer feedback, the recognition consistently highlights the company’s unwavering commitment to delivering high-quality results and unparalleled customer satisfaction in a shifting industry landscape. For details on Worldwide’s awards, click here .

For an overview of Worldwide’s Phase I service offerings, including its full suite of clinical pharmacology studies, click here .

About Worldwide Clinical Trials: Worldwide Clinical Trials (Worldwide) is a full-service global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Worldwide’s capabilities include bioanalytical laboratory services, Phase I-IV clinical trials, and post-approval and real-world evidence studies – all powered by an accessible team of clinicians, scientists, and researchers who bring first-hand expertise and a collaborative, personalized approach to each clinical program. Worldwide is therapeutically focused on neuroscience, oncology, rare diseases, and cardiometabolic and inflammatory disease. Its global footprint spans nearly 60 countries with more than 3,500 team members. For more information, visit www.worldwide.com .

Media Contact: Jill Mastrangelo [email protected]

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Worldwide clinical trials ranked as top cro for overall performance in 2024 industry standard research phase ii/iii benchmarking report, worldwide clinical trials recognized with coveted 2024 cro leadership awards based on customer feedback for 11th consecutive year, worldwide clinical trials expands clinical pharmacology unit pharmacy to enhance customer experience; adds efficiencies and decreases timelines.

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Changing what it means to work with a CRO.™

At Rho, we believe expertise is everything. With a demonstrated track record of success, we guide our clients through the most appropriate program strategies, navigate the unique challenges of clinical trials, and drive development of the high-quality marketing applications demanded by regulatory authorities.

Our experts take clients beyond procedural operations and into truly proactive problem-solving. Through a collaborative approach and individualized attention, our focus is advancing your program so that together, we can help heal the world.

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List of Contract Research Organizations in India

Featured cros.

Celero provides optimal returns to innovative biotechs & pharmaceutical companies by addressing unmet needs, accelerating clinical development and commercialising innovative healthcare products.Trial mismanagement is the main reason why 85%-90% o...

Innovate Research

Innovate Research stands as a leading Contract Research Organization (CRO) dedicated to providing comprehensive services in the dynamic field of clinical research, established in January 2014 With a strategic presence across the globe, our offices ar...

ACROSS Global in India

E-mail:   [email protected]

Web:   www.across.global

SIRO Clinpharm

Address: Kalpataru Prime, 1st Floor, Unit nos. 3 and 4, Plot no D-3, Road no 16, Wagle Industrial Estate, Thane (West) – 400 604, Maharashtra

Phone:   +912261088000

ProRelix Research

Since 2014 ProRelix Research has been supporting our clients with outstanding clinical research services. The successful growth of ProRelix Research has been achieved by putting high quality and client focus at the heart of everything we do.We levera...

Local, small- and mid-size Contract Research Organizations in India

Aagami, Inc. is a life sciences consulting firm based in the suburbs of Chicago which offers, Strategic Consulting Services Business Development support in regions where you are unable to reach out due to bandwidth Technology Licensing Se... View full profile

• United States

Abiogenesis Clinpharm has been helping pharmaceutical companies transform their ideas and concepts into successful products. We are a highly focused team of professionals who understand how to prepare, manage and conduct clinical trials. Our core act... View full profile

Accelsiors is a scientifically-driven CRO committed to serving the needs of its Sponsors with the highest level of quality. We provide a full array of services and pride ourselves on having ready access to treatment naive patient populations. From co... View full profile

Accutest is a global independent and internationally accredited Contract Research Organisation (“CRO”) founded in 1998. We are offering services to customers around the world with operations in India, across Asia, and in Brazil. Accutest is the marke... View full profile

Actimus Biosciences as a knowledge based CRO, was established in the year 2005. The facilities are located in Visakhapatnam, Andhra Pradesh, India. We pride ourselves by providing most reliable and quality services to pharmaceutical companies in thei... View full profile

APCER Life Sciences is committed to improving health in partnership with its clients. We bring together safety, medical, regulatory, and technology resources to ensure that patients receive the safest, most effective therapies possible. To achieve th... View full profile

• United Kingdom

Asiatic Clinical Research is a full service clinical research organization (CRO) headquartered in Bangalore, India. We focus on Phase II - IV clinical trial support to pharmaceutical, biotechnology and medical device companies. Our strength is in str... View full profile

Astron Research Limited, a leading IP oriented pharma contract research organization, is a fast growing Pharma Contract Research Organisation (CRO) with a strong quest to deliver best services to the rapidly growing Healthcare industry and has embark... View full profile

AXIS is an efficient, metric based clinical research provider with a global footprint of operations. Our mandate recognizes the need within the medical research community for quality clinical services backed by experience, ICH/GCP training, protocol... View full profile

Started in 2005 Bioaxis DNA Research Centre (BDRC) private limited is a top level CRO in life sciences with a vast range of services in Biotechnology, Bioinformatics, Forensic Science and Clinical Research. BDRC is one of the most trusted DNA Testing... View full profile

Catalyst Clinical Services Pvt. Ltd. is a Contract Research Organization that acts as a strategic partner to the healthcare organizations (Pharma/Biotech companies, Research and Academic Institutions) making them winner by building on their core comp... View full profile

At Clinexa, we are in a constant pursuit to identify the best ways to pass value to our clients. We challenge ourselves and our stakeholders to create new and innovative models that take into consideration the needs of today’s clinical development ne... View full profile

CSSi was founded in 2005 as Clinical Site Services to serve individual sites with their patient recruitment needs, later expanding into a major global centralized patient recruitment company. A leader in the industry, CSSi delivers strategic patient... View full profile

CliniExperts Research Services a prominent Indian CRO with a decade of experience, leads in clinical research. Our expertise spans clinical trials, biometrics, and regulatory approvals, with a focus on drugs, Medica Devices, IVDs, Biologicals, and va... View full profile

Cliniminds was established in year 2004, by a group of professionals from Clinical Research, Pharmaceutical industry and Healthcare industry with rich and varied experience at senior management levels. Cliniminds offers Educational & Training Pro... View full profile

CliniRx is a full service mid-size CRO that provides comprehensive end- to- end solutions for clinical studies. CliniRx’s services include Phase II –III and late Phase (Phase IV) across numerous therapeutic areas and specialties.These specialty areas... View full profile

D2L Pharma Research Solutions is a leading force in opinion leader engagement. Established in the year 2007, D2L ‘Discovery to Launch’ has been at the forefront of providing exemplary service to the pharmaceutical, biotechnology, and medical communic... View full profile

DIL Ltd. (earlier known as Duphar-Interfran Ltd.) is a well-respected public listed company. It has built a stellar reputation for itself in the arenas of pharmaceuticals, biotechnology, environmental solutions and other segments including Entertainm... View full profile

Dishman is the global outsourcing partner for the pharmaceutical industry offering a portfolio of development, scale-up and manufacturing services. The products and services offered span customers’ needs from chemical development to commercial manufa... View full profile

Divi’s has been established for more than 29 years in Hyderabad, India with two manufacturing units and is among the top pharmaceuticals companies in India. Divi’s is recognized as a ‘Reliable Supplier of generic APIs (Active pharmaceuticals ingredi... View full profile

Dabur Research Foundation (DRF) is an Indian Contract Research Organization offering pre-clinical services in Drug Discovery and Development, ranging from identification of potential lead molecules, drug development to IND enabling studies. We offer... View full profile

endpoint is the destination for people who are passionate about delivering the most innovative and high-quality IRT solutions for clinical trials. We find purpose through hard work and a commitment to excellence, resulting in a competitive advantage... View full profile

Eurofins Advinus is a R&D services company that supports the discovery and development of compounds for diverse industries including Pharmaceuticals, Biologicals, Agrochemicals, Nutraceuticals and Cosmetics. Eurofins Advinus is part of Eurofins S... View full profile

Global Drug Development (GDD) Experts is the Site Management Organization (SMO) of choice in India. GDD is a US-based company, and brings global expertise in quality assurance and patient enrollment to the Indian SMO market. Unmatched in therapeutic... View full profile

GVK BIO, a leading Contract Research & Development Organization – CRDO that services the global Biopharma industry; is headquartered in Hyderabad, India with operations in four sites including California, USA. Established in 2001, GVK BIO has ove... View full profile

• Netherlands

HaleUS provides services to help life science and pharmaceutical companies with a vision of Scientific expedition toward better cure. We are providing end to end services in Clinical Trial; starting from Medical writing to regulatory approval. Our te... View full profile

Hi Tech BioSciences India Ltd. is a prominent supplier of high end products and research based solutions in the arena of nutraceuticals and biocatalysis. Founded by Dr. Raghavendra Gaikaiwari in 2007, Hi Tech BioSciences has in a short period of time... View full profile

Founded in 1995, Indus Biotech is a pioneer in deriving science based dietary ingredients from food chain raw materials through revolutionary patented technology. Our products are subjected to the highest levels of scientific rigour. We understand th... View full profile

Infoclin LLP (A research management company) Introduction Infoclin LLP is a clinical research management company, based at Kolkata, India & business development center in Mumbai, India. Initially it was set up as site Network Company in the name... View full profile

Innovate Research stands as a leading Contract Research Organization (CRO) dedicated to providing comprehensive services in the dynamic field of clinical research, established in January 2014 With a strategic presence across the globe, our offices ar... View full profile

• United Arab Emirates

The International Pharma Trials group is committed to the highest standards of clinical excellence and scientific expertise. View full profile

A Contract Research Organization (CRO), INTOX performs a wide range of studies, including Toxicological, Mutagenicity, Ecotoxicological and Chemical, for Pharmaceutical, Crop Protection / Agrochemical, Biotechnological, Chemical and Medical devices i... View full profile

InrexTest facilitates and coordinates pharmaceutical and medical device studies through our team of internal experts coupled with top quality labs supporting preclinical and clinical testing at every stage of development. At InrexTest, we understand... View full profile

JRF Global offers comprehensive non clinical GLP research services for regulatory submissions, worldwide. We offer fast, transparent, cost-effective, and hassle-free services in Toxicology, Eco-toxicology, Chemistry, Environmental Fate and Metabolism... View full profile

JSS Medical Research is a full-service CRO built on a foundation of epidemiological and scientific expertise, with a strong network of academic affiliations and over 30 years of experience in multiple therapeutic areas. We are an international Canad... View full profile

Kemwell is a contract biologics development and CMO company providing services to global biopharmaceutical organizations. Kemwell facilities, located in Bangalore, India, are designed and developed with technological support from a leading German pha... View full profile

KPS Clinical Services Pvt. Ltd. is set up by Shri Ratiram ji Group with an aim to become one of the India's leading Contract Research Organization (CRO). Our commitment is to improve the quality of human life & to provide world-class clinical res... View full profile

Labnetworx is a consulting company that operates at the interface of Healthcare, Life Sciences, Pharmaceuticals and Information Technology. We offer our customers solutions designed to meet the needs of today and tomorrow.... View full profile

We, Lambda Therapeutic Research Limited are a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad – India, with facilities and operations in Mehsana (India), Warsaw (Poland), London (UK), Pittsburgh (USA), Las Vegas (USA) a... View full profile

Laxai Life Sciences Pvt. Ltd. was established in the year 2007, with a vision to accelerate the discovery chemistry campaign of global pharmaceutical companies, by supporting the high quality intended compounds in reduced pricing and timeline. With t... View full profile

Max India, a part of the leading Indian conglomerate Max Group, has a presence in the senior living and healthcare industry. It is the holding company of Antara Senior Living and an equal joint venture partner with a 49.7% in Max Healthcare along wit... View full profile

Maya Clinicals is a Northern California CRO with an extensive network of sites, MD’s, and specialists in India. We are focused on working with Bio-Pharma start-ups and Pharma companies in a unique and flexible co-development model to accelerate drug... View full profile

We are one of the leading diagnostics companies in India, by revenue, as of March 31, 2018 (Source: Frost & Sullivan). We have widespread presence across 18 states in India, as of March 31, 2018, with leadership position in west and south India (... View full profile

MMS is a place where years of proven success have guided sponsors through their data services and regulatory submissions goals. When MMS takes on a project, colleagues become ingrained in that sponsor – taking on a greater level of care and guiding t... View full profile

In today’s increasingly complex clinical development environment, life sciences companies are faced with pressures from regulators, payers, and the public to manage clinical trials that are safe, cost-effective, and informed by big data and technolog... View full profile

“Ocimum Biosolution” is a comprehensive Integrated Life Science Informatics solutions provider with service offerings that span Sample and Data Management (LIMS, Biologics Data Management), Genomics Data Analysis Services such as Gene Expression, Gen... View full profile

Navigating the CRO landscape can be difficult for biotech companies that vastly rely on outsourcing as the differentiation between CROs seems marginal and confusing at times. Orphan Reach is different: We are a boutique service provider solely focuse... View full profile

Pharmaffiliates Analytics and Synthetics P. Ltd., a Research Based Organization is a gigantic name in the global market, which offers services to Pharmaceutical industry, Biotechnology industry, API manufacturers, Bulk drug suppliers, clinical CROs,... View full profile

Premas Biotech is an emerging trendsetter in next generation protein expression and process development for scale up. With over 13 years of experience and a world-class team of scientists, we enable customers steer therapeutic development in a quicke... View full profile

Since 2014 ProRelix Research has been supporting our clients with outstanding clinical research services. The successful growth of ProRelix Research has been achieved by putting high quality and client focus at the heart of everything we do.We levera... View full profile

Originally founded in Basel, Switzerland in 1977, RCC has grown into one of Europe’s largest pre-clinical research providers by developing services that meets the needs of worldwide clients. RCC Laboratories India was established in November 2005 and... View full profile

Reliance Life Sciences is a research-driven organization developing business opportunities in bio-therapeutics (plasma proteins, biosimilars and novel proteins), pharmaceuticals (later-generation, oncology generics), clinical research services, regen... View full profile

Sai Life Sciences delivers advanced Discovery, Contract Development and Manufacturing Solutions, through a broad suite of expert capabilities across the molecular lifecycle.We are an ideal drug discovery, development and manufacturing partner. Our ph... View full profile

ScientiaBio, a young and energetic Indian CRO (established in March 2010), with a global client base, is a dominant player in the Phama Emerging Nations. We provide precise and targeted solutions to different areas of pharmaceutical development prima... View full profile

Spectrum Clinical Research is an one-of-its-kind patient-focused drug development organization. Our aim is to provide quality clinical research support to pharmaceutical companies and Contract Research Organizations in order to facilitate the develop... View full profile

Strand offers clinical research and development services to pharmaceutical and biotechnology companies in the areas of clinical trial management, biomarker discovery, and validation. Led by a team of specialist oncopathologists, molecular biologists,... View full profile

Incorporated in 1990, Strides Pharma Science Limited is a global pharmaceutical company headquartered in Bangalore, India. The Company has two business verticals, viz., Regulated Markets and Emerging Markets. Strides has a global manufacturing footpr... View full profile

SyMetric (a brand owned by Achiral Systems Private Limited) is the brainchild of a group of highly-skilled professionals with in-depth exposure to the IT Software and Clinical Research Industries. With more than 120 person years of combined relevant... View full profile

Established in 2008 by Pharma industry experts Technology driven organization with a flexible approach. Founded by scientists with proven industrial track record. Expertise in Process Research/Development and scale-up (non-GMP and cGMP). Research... View full profile

Synchron was started by a group of pharmaceutical professionals in 1998. Today Synchron is a leading Contract Research Organization in India providing broad range of clinical research services from phase I to phase IV, including : Bioavailability... View full profile

TCG Lifesciences Private Limited (formerly “Chembiotek Research International”) is a leading Contract Research and Manufacturing Services (“CRAMS”) company in the area of early drug discovery and development. We started our operations in the year 200... View full profile

Whether in the race of bringing that best-in-class treatment to patients or conducting post-marketing research to generate real-world evidence, you can count on Tech Observer to reach the goal. We can help in clinical operations, data management, sta... View full profile

The Sanmar Group has come a long way since its first international foray back in the 1970s. Since then, the Group has set the benchmark for global partnerships in a range of industry segments. These are partnerships based on trust, transparency and r... View full profile

Incorporated in 1996, SIRO Clinpharm Private Limited is a Clinical Research Organisation supporting trials from Phase II to Phase IV and beyond post-launch of products. SIRO offers a range of services, from clinical operations to data services, data... View full profile

Vedic Lifesciences has been helping food supplement and ingredient companies substantiate health claims for North America, Europe and Asia for the last two decades. As a contract research organization (CRO), we have completed more than 400 clinical a... View full profile

Veeda Clinical Research Pvt. Ltd. derives its name from the Sanskrit word 'Veda', meaning knowledge or wisdom. The name represents our firm belief in scientific knowledge and technical expertise to provide quality solutions. We are innovators with a... View full profile

VIMTA was established in 1984 and is a company driven by its vision and enduring strength. VIMTA’s business landscape includes analytical, clinical, preclinical services to life sciences industries; quality and safety testing for food and beverage in... View full profile

Vivo Bio Tech is a full service CRO offering drug development & discovery services to pharmaceutical & biotech companies world-wide in accordance with OECD - GLP, AAALAC & IND guidelines. The company offers services in the areas of In viv... View full profile

Zenovel is a highly reputed, credible, and reliable partner for GxP (GCP/GMP/GLP) Services, Regulatory Affairs and Pharmacovigilance Services.Zenovel has been a partner of choice for many global pharma companies for their different outsourcing need i... View full profile

Global Contract Research Organizations in India

Since 1975, ACM Global Laboratories has been a recognized leader in both medical diagnostic and global clinical trial testing services. With wholly owned facilities in New York, England, Shanghai China, Mumbai India and Singapore, we operate in more... View full profile

ACROSS Global is a unique, full-service, comprehensive alliance of qualified CROs and Specialist Service Providers dedicated to providing a professional, cost-effective, focused, and seamless service to the pharmaceutical, biopharma and medical devic... View full profile

• Bosnia & Herzegovina
• Congo, DR of
• Philippines
• Saudi Arabia
• South Africa
• South Korea
• Switzerland

BioReliance provides testing and manufacturing services to pharmaceutical and biopharmaceutical companies that span the product cycle from early pre-clinical development to licensed production. Our goal is to advance the development and delivery of h... View full profile

A global, full-service contract research organization. We take your trials personally. dMed Global, a full-service Clinical Contract Research Organization (CRO) based in Shanghai, China and Clinipace Incorporated, a full-service Clinical CRO with hea... View full profile

• Czech Republic

Celero provides optimal returns to innovative biotechs & pharmaceutical companies by addressing unmet needs, accelerating clinical development and commercialising innovative healthcare products.Trial mismanagement is the main reason why 85%-90% o... View full profile

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guides us in all that we do, and we approach each day with the knowledge that our work h... View full profile

As a provider of comprehensive Phase I through IV clinical trial management, clinical pharmacology, patient access solutions and other enabling services, Fortrea partners with emerging and large biopharma and medical device and diagnostic companies t... View full profile

• New Zealand

FMD K&L is a global contract research organization supporting data management, biostatistics, statistical programming, clinical operations, regulatory affairs, safety, pharmacovigilance, toxicology, medical affairs, medical writing, quality, risk... View full profile

Global Clinical Trials, LLC is a full-service CRO with offices and operations in the United States, Europe and Asia. Our professional staff have been sharing their unique experience and utilizing established contacts with the key opinion leaders (KOL... View full profile

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We are a global provider of consulting, and outsourced developme... View full profile

IMS Health and Quintiles are now IQVIA, a world leader in using data, technology, advanced analytics and expertise to help customers drive healthcare - and human health - forward. Together with the companies we serve, we are enabling a more modern, m... View full profile

MakroCare is expert strategic development and commercialization global partner for pharmaceutical, biotechnology and medical device industries. Our experience, programs and processes bring a new dimension to development strategy, regulatory/risk plan... View full profile

Medidee’s CRO (Clinical Research Organisation) services are backed up by decades of experience in the fields of medical device engineering, quality and regulatory affairs. This unique combination of all relevant competences supports all aspects of yo... View full profile

Our unique global partnering philosophy emphasizes an uncompromising commitment to clinical research and to the highest level of ethical standards and performance in our jobs. We are selective about the projects we engage in because we are devoted to... View full profile

Headquartered in Australia and focused exclusively on the Asia Pacific, Novotech is internationally recognized as a leading regional full-service CRO. With the increasing pace of globalization in drug development, Novotech’s expertise in the vibrant... View full profile

For over 35 years, PAREXEL has proven to be a trusted partner for the complex development journey required of biopharmaceutical and medical device companies. We’re also an astute guide, able to simplify that journey for our clients, so safe new produ... View full profile

PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and go... View full profile

ProPharma Group partners with life science companies to solve their complex challenges. As an extension of your team, we care about not only the progression of your products through the development lifecycle, but also the safety of your products and... View full profile

Our mission is to be the best CRO in the world as measured by our employees, clients, investigators, and vendors. Our teams work tirelessly to ensure that we deliver on time and on budget. You will always know what's going on with your study when you... View full profile

QPS was founded in 1995. Today, the company is considered one of the top CROs in the world. QPS is a GLP/GCP-compliant contract research organization (CRO) supporting discovery, preclinical and clinical drug development. QPS provides quality services... View full profile

Quanticate is a leading global data-focused Clinical Research Organization (CRO) which may also be known as a 'Biometric CRO'. Quanticate is primarily focused on the management, analysis and reporting of data from clinical trials and post-marketing s... View full profile

We are the world’s leading provider of diagnostic testing, information and services that patients and doctors need to make better healthcare decisions. Our services range from routine blood tests — such as total cholesterol, Pap testing and white blo... View full profile

Life sciences services from SGS – optimize your development timelines to get medicines and medical devices to market quickly and safely. There is no other area of business that is more heavily regulated than the development, testing and distribution... View full profile

• Burkina Faso
• Cote d'Ivoire
• Dominican Republic
• El Salvador
• Equatorial Guinea
• Papua New Guinea
• Saint Lucia
• Trinidad & Tobago
• Turkmenistan

Spade Health is a medical market research company that provides clinical research management services to pharmaceuticals and end clients. Spade Health, is focused on providing biotech and pharmaceutical companies with an assortment of services tailor... View full profile

Syneos Health (Nasdaq:SYNH) is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, strategically blending clinical development, medical affairs a... View full profile

TAKE Solutions delivers domain-intensive services in Life Sciences and Supply Chain Management. In the fast-growing Life Sciences space, TAKE offers clients a unique combination of full-service Clinical, Regulatory and Safety services backed by uniqu... View full profile

List of CROs by location

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Pharmaceutical Sciences and Clinical Supply

"altering the course of human health by transforming , science and technology into meaningful drug product s ", the pharmaceutical sciences and clinical supply organization is a division within merck research laboratories, responsible for transforming science and technology into meaningful drug products from conception to market to alter the course of human health. our value lies in inventing and developing new drug products for merck., join our talent community to stay connected and receive updates on the latest job opportunities., our organization, partner across the company to optimize the value of our therapies through drug product design and delivery, maintain good manufacturing practices infrastructure and sourcing network for oral, sterile and speciality drug products. , maintain an international supply chain  of clinical trial materials through packaging,  labeling, shipping and trade compliance, worldwide operations, rahway, new jersey, west point, pennsylvania, boston, massachusetts, san francisco,  california  , switzerland, europe, our commitment to talent development, join our talent community today., receive updates on career opportunities tailored to you., connect with us on social, beware of hiring scams. review our applicant notice ..