Experienced Clinical Research Associate
Core
Verify subject rights and well-being, ensure trial data accuracy and compliance with GCP/protocol, and conduct site monitoring visits for clinical trials.
Role type
Experienced Clinical Research Associate (CRA)
Builds
Clinical trial monitoring and data verification for biotechnology, pharmaceutical, and medical device clients
Domain
Clinical Research / Clinical Operations
Deliverable
physical/clinical work
Required skills
Clinical monitoring, GCP compliance, Protocol adherence, Site qualification, Study initiation, Study close-out, Data verification, Subject rights protection, Mentorship, SOP implementation
Preferred skills
Lead CRA capability, Training facilitation, Innovation in solutions
Technologies
ClinTrak Monitoring Portal
Responsibilities
Verify subject rights and well-being; Ensure trial data accuracy and compliance; Conduct qualification, initiation, routine, and close-out site visits; Serve as primary resource to investigators; Mentor new CRAs; Maintain study databases and visit reports.