Clinical Research Coordinator (On-site)
Core
Coordinate day-to-day clinical trial activities, ensuring protocol compliance, data integrity, and operational efficiency while supporting the Principal Investigator.
Role type
Senior Clinical Research Coordinator (IC)
Builds
Clinical trials for global biopharmaceutical, biotechnology, and medical device organizations
Domain
Healthcare / Clinical Research
Required skills
Clinical trial execution, protocol compliance, data management, regulatory documentation, participant screening, team mentorship, study start-up and close-out, GCP guidelines, HIPAA compliance, workload prioritization
Preferred skills
Phlebotomy, GCP Certification, Advanced CRC certification, familiarity with Code of Federal Regulations
Technologies
Case report forms, study charts, regulatory documentation systems
Responsibilities
Screen and review potential study participant eligibility; maintain accurate case report forms and regulatory documentation; provide mentorship and oversight to research staff; collect and enter study data; assist with study start-up, maintenance, and close-out; collaborate with investigators, sponsors, and CROs
Seniority
Mid-level, hands-on IC