Advance AbbVie’s pipeline by striving for excellence in clinical research
Partners with the investigator and site staff for meaningful and effective engagements
Focus on site clinical research that ensures appropriate conduct of the trial
Drive improvement in data integrity, compliance, overall study performance and customer experience
Primary point of contact for the investigative site, providing contextual information on the clinical trials
Align, train and motivate the site staff and principal investigator
Conducts site evaluation, training, routine and site closure monitoring activities
Gather local/site insights and utilize site engagement tools to report progress
Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey
Responsible for continuous risk-assessment proactively, monitor activities conducted by clinical sites
Ensure quality of data submitted from study sites
Identify, evaluate and recommend new/potential investigators/sites under supervision

Bachelor’s degree required; health related preferred (e.g. Medical, Scientific, Nursing, Pharmacy)
Clinically related experience, preferably in clinical research monitoring, coordinating or data management
Knowledge of appropriate therapeutic area indications is preferred
Ability to understand and 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
Ability to use functional expertise with appropriate guidance
Interpersonal skills with strong written, verbal, active listening and presentation skills
Self-motivated individual focused on delivering timely and quality outcomes in a fast-paced environment.

Clinical Research Associate I

Key skills