Clinical Research Associate I
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 I (IC)
Builds
Clinical studies for AbbVie
Domain
Healthcare / Clinical Trials
Deliverable
physical/clinical work (via careerplan.io/jobs/3743990015832254-clinical-research-associate-i-at-abbvie)
Required skills
Site qualification, protocol adherence, regulatory compliance (GCP/ICH), data quality assurance, safety monitoring, investigator management, site identification, training
Preferred skills
Health-related tertiary qualification, Clinical Trials Master's Degree, 6 months independent monitoring or Study Coordinator experience
Technologies
None stated
Responsibilities
Conduct site qualification, initiation, interim monitoring, and closeout visits; ensure regulatory inspection readiness; manage investigator payments and agreements; identify and evaluate potential investigators/sites; train site personnel on protocols and regulations.
Seniority
Entry-level (1 year experience)