Clinical Research Associate
Core
Partner with clinical investigative sites to ensure successful execution of Phase 1-4 clinical studies, driving data integrity, compliance, and study performance.
Role type
Clinical Research Associate (Site Monitoring)
Builds
Clinical trial execution for AbbVie's pipeline in immunology, oncology, and neuroscience
Domain
Clinical Research / Pharmaceutical
Deliverable
client delivery
Required skills
Site qualification and monitoring, Protocol adherence, Regulatory compliance (GCP/ICH), Data quality assurance, Safety event reporting, Investigator relationship management, Site identification and evaluation
Preferred skills
Health-related tertiary qualification (Medical, Scientific, Nursing), Experience in on-site monitoring of investigational drug or device trials, In-depth knowledge of therapeutic indications
Technologies
None stated
Responsibilities
Monitor clinical investigative sites for protocol adherence and regulatory compliance; Conduct site qualification, initiation, interim, and closeout visits; Ensure quality and timely submission of data and safety event reporting; Train site personnel on protocol and regulations; Manage investigator payments and negotiate agreements; Identify and evaluate potential new investigators or sites
Seniority
Mid-level, hands-on IC