Clinical Research Associate

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

• Considered as the primary Sponsor point of contact for the investigative site, provides contextual 

information on the clinical trials, connects stakeholder to the investigative sites and strengthens 

AbbVie’s positioning.

• Aligns, trains and motivates the site staff and principal investigator with support as needed on the 

goals of the clinical trial program, protocol, and patient treatment principles for the trial ensuring a 

trusted partnership.

• Conducts site evaluation, site training, routine on-site and off-site monitoring, and site closure 

activities with support as needed, in compliance to the protocol and monitoring plans and accordance

with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard 

•Operating Procedures (SOPs), and to quality standards in conducting clinical research, ensuring 

safety and protection of study subjects.

• Customize site engagement strategy for assigned study (ies) with support as needed. Gather 

local/site insights and utilize site engagement tracking tools, to report/track progress and measure 

impact of that strategy.

• Fundamental level of competency connecting the study protocol, scientific principles and clinical 

trial requirements to the day-to-day clinical trial execution activities. Evaluate and ensure effective 

recruitment and retention techniques/plans based on the patient disease journey. Develop solid 

knowledge of therapeutic area, asset and clinical landscape / patient journey to enable successful 

patient recruitment and overall protocol compliance.

•Responsible for continuous risk-assessment proactively, and in collaboration with Central 

•Monitoring team, monitor activities conducted by clinical sites to detect early overall study 

performance or patient safety issues. Ability to think critically to resolve site risk signals while having 

robust understanding of site processes to drive study execution.

• Identifies, evaluates and recommends new/potential investigators/sites with support as needed 

from more experienced Site Monitors.

• 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 audit and regulatory inspection readiness at assigned clinical site at all times.

• Manages investigator payments as per executed contract obligations, as applicable.

• Appropriate tertiary qualification in health-related disciplines (e.g., Medical, Scientific, Pharmacy,

Nursing) preferred or experience or equivalent work experience.

• Minimum of 3-5 years of direct monitoring experience in clinical trials, with significant experience 

in interventional studies.

• Previous experience managing sites in global clinical trials (multi-country studies), including start

-up, monitoring, and close-out activities.

• Clinically related experience, in clinical research coordinating or data management preferred.

• Knowledge of appropriate therapeutic area indications is preferred with the ability to understand a

nd apply scientific concepts as they relate to the conduct of clinical trials.

• Knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines

and applicable policies.

• Able to work collaboratively and cross functionally to develop and sustain working relationships.

• Demonstrate planning and organizational skills and the ability to work effectively and efficiently in a

dynamic environment with competing projects and deadlines

• Ability to leverage technology, tools and resources to provide customer centric support based on

the health of the site.

• Interpersonal skills with strong written, verbal, active listening and presentation skills, with ability to

establish and leverage site relationships and trusted partnerships through engagement, motivation,

and training.

• Ability to use functional expertise with appropriate guidance, leverage critical thinking skills and

apply good judgement to address clinical site issues.

• Acts with integrity in accordance with AbbVie code of business conduct and leadership values. Self motivated individual focused on delivering timely and quality outcomes in a fast-paced environment.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

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