clinical research associate abbvie salary

AbbVie Inc. Clinical Research Lead Scientist Salary in the United States

How much does a Clinical Research Lead Scientist make at companies like AbbVie Inc. in the United States? The average salary for Clinical Research Lead Scientist at companies like AbbVie Inc. in the United States is $102,600 as of May 28, 2024, but the range typically falls between $87,000 and $123,700 . Salary ranges can vary widely depending on many important factors, including education, certifications, additional skills, the number of years you have spent in your profession. With more online, real-time compensation data than any other website, Salary.com helps you determine your exact pay target.  View the Cost of Living in Major Cities

About AbbVie Inc.

Browse other Companies in the Biotechnology Industry

View abbvie inc. Salary

What does a Clinical Research Lead Scientist do at companies like AbbVie Inc.?

The Clinical Research Lead Scientist proposes, plans, organizes and executes experiments and research. Assumes lead role in various clinical research projects. Being a Clinical Research Lead Scientist summarizes findings in reports and communicates results. Secures grants and funding for research and is responsible for controlling budgets. In addition, Clinical Research Lead Scientist interacts with other scientists within and outside of the organization. Provides recommendations that influence extensive clinical research activities. Requires an advanced degree. Typically reports to head of a unit/department. Being a Clinical Research Lead Scientist work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. Working as a Clinical Research Lead Scientist typically requires 4 -7 years of related experience. (Copyright 2024 Salary.com)

See user submitted job responsibilities for Clinical Research Lead Scientist.

Learn More About

Associate Scientist, R&D

Natera - Austin, TX

Data Scientist / Statistician

Active Motif Inc - Carlsbad, CA

Manager of Clinical Innovation (Clinical Scientist I)

AbbVie - Irvine, CA

Director, Biological Research/Senior Principal Research Scientist

Allergan Aesthetics - Irvine, CA

Understand the total compensation opportunity for Clinical Research Lead Scientist at companies like AbbVie Inc., base salary plus other pay elements

Average base salary.

Core compensation

Average Total Cash Compensation

Includes base and annual incentives

Similar Job Titles:

Search Job Openings

What does a clinical research lead scientist do, are you an hr manager or compensation specialist.

Salary.com's CompAnalyst platform offers:

• Detailed skills and competency reports for specific positions
• Job and employee pricing reports
• Compensation data tools, salary structures, surveys and benchmarks.

Level of Education

• Clinical Research Lead Scientist Salaries with a JD, MD, PhD or Equivalent

Average Clinical Research Associate (CRA) Salary at Abbvie, Inc in Chicago, Illinois

The average salary for a Clinical Research Associate (CRA) is $67,507 in 2024

Featured Content

What do clinical research associate (cra)s do.

Clinical research associates (CRA) are responsible for assisting in the clinical research process, providing advanced technical expertise in steps such as handling supplies, ordering tests, and collecting results, presenting specific research information to the public, and a variety of administrative tasks. CRAs must follow strict privacy and safety regulations to prevent problems with subjects and ethical concerns; they must also be organized and pay close attention to detail when conducting …Read more

Common Health Benefits for a Clinical Research Associate (CRA)

Gender breakdown for clinical research associate (cra)s.

FAQs About Clinical Research Associate (CRA)s

What is the highest pay for clinical research associate (cra)s in chicago.

Our data indicates that the highest pay for a Clinical Research Associate (CRA) in Chicago is $NaN / year

What is the lowest pay for Clinical Research Associate (CRA)s in Chicago?

Our data indicates that the lowest pay for a Clinical Research Associate (CRA) in Chicago is $NaN / year

How can Clinical Research Associate (CRA)s increase their salary?

Increasing your pay as a Clinical Research Associate (CRA) is possible in different ways. Change of employer: Consider a career move to a new employer that is willing to pay higher for your skills. Level of Education: Gaining advanced degrees may allow this role to increase their income potential and qualify for promotions. Managing Experience: If you are a Clinical Research Associate (CRA) that oversees more junior Clinical Research Associate (CRA)s, this experience can increase the likelihood to earn more.

Clinical Research Associate

__jobinformationwidget.freetext.LocationText__

Shanghai, SH

• Function: Research & Development
• Area of Interest: Analytical Research & Development
• Job Type Full-time
• Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research.
• Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs) and business processes.
• Overviews the overall activities of site personnel over whom there is no direct authority and motivates/influences them to meet study objectives. proactively manages the site and ensures action plans are put into place as needed to ensure compliance. Ensures regulatory inspection readiness at assigned clinical sites.
• Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
• Ensures safety and protection of study subjects through compliance with the study monitoring plan, AbbVie SOPs, ICH Guidelines, and applicable regulations.
• Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members.
• Manages investigator payments as per executed contract obligations. Negotiates investigator/ hospital agreements with stakeholders. Maintain and complete own expense reports as per local and applicable guidelines.
• Identifies, evaluates and recommends new/potential investigators/sites on an on going basis. Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators.
• Appropriate tertiary qualification, health related (e.g., Medical, Scientific, Nursing) preferred.
• Minimum of 1 year of clinically-related experience, of which a period of 6 months is preferable in clinical research monitoring. Experience in on-site monitoring of investigational drug or device trials is required
• Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials.
• Current in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines and applicable regulations.
• Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, understand and follow work processes within the assigned function.
• Strong analytical and conceptual capabilities, interpersonal skills, and ability to communicate with clarity. Ability to address study related clinical site issues with appropriate guidance and initiates and communicate corrective action as indicated. Ability to use functional expertise and exercise good judgment.
• Demonstrated business ethics and integrity.

AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.  It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

• Travel: Yes, 25% of the Time