Clinical Research Associate II
Core
Monitor clinical investigative sites to ensure successful execution of Phase 1-4 study protocols, ensuring adherence to regulations and quality standards.
Role type
Mid-level Clinical Research Associate (Site Monitoring)
Builds
Clinical studies for AbbVie's therapeutic areas (immunology, oncology, neuroscience)
Domain
Biopharmaceuticals / Clinical Research
Deliverable
client delivery
Required skills
Site monitoring, regulatory compliance (GCP/ICH), site qualification, data quality assurance, safety monitoring, investigator contract management, site identification
Preferred skills
Health-related tertiary qualification (Medical, Scientific, Nursing), therapeutic area knowledge
Technologies
None stated
Responsibilities
Conduct site qualification, initiation, interim monitoring, and closeout visits; ensure regulatory inspection readiness; manage investigator payments and negotiate agreements; train site personnel on protocols; identify potential new investigators/sites
Seniority
Mid-level, hands-on IC