Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients
Partners with study teams, AbbVie internal R&D stakeholders, investigators, and site staff for meaningful and effective engagements positioning AbbVie as the partner of choice in clinical trials
Conducts site evaluation, site training, routine on-site and off-site monitoring, and site closure monitoring activities with compliance to the protocol and monitoring plans
Gather local/site insights and utilize site engagement tools to report/track progress and measure impact of that strategy
Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey to enable successful patient recruitment and overall protocol compliance
Supports local onboarding of more junior CRAs
Responsible for activities as assigned by manager

Appropriate tertiary qualification in health related disciplines (e.g., Medical, Scientific, Pharmacy, Nursing)
Minimum of 3 years of clinically related experience, of which a period of 5 years is preferable in independent clinical research monitoring of investigational drug or device trials in any therapeutic area
Familiar with risk‐based monitoring approach, onsite and offsite monitoring
Knowledge of appropriate therapeutic area indications with the ability to understand and apply scientific concepts as they relate to the conduct of clinical trials
Superior knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies
Demonstrate advanced communication skills and superior cross-functional collaboration skills among internal and external stakeholders
Demonstrate superior 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
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.

Senior Clinical Research Associate

Key skills