Clinical Research Associate 2
Core
Monitors clinical investigative sites to ensure successful execution of protocols, adherence to regulations, and quality standards for Phase 1-4 studies.
Role type
Clinical Research Associate 2 (IC)
Builds
Clinical trial data and safety reports for AbbVie studies
Domain
Biopharmaceuticals / Clinical Research
Deliverable
client delivery
Required skills
Site monitoring, regulatory compliance (GCP/ICH), data quality assurance, safety event reporting, site qualification, investigator contract management, site identification
Preferred skills
Tertiary health-related qualification, independent monitoring experience, therapeutic area knowledge
Technologies
None stated
Responsibilities
Conduct site qualification, initiation, interim, and closeout visits; ensure data quality and timely submission; train site personnel on protocols; manage investigator payments and agreements; identify potential new sites
Seniority
Mid-level, hands-on IC
