Clinical Research Coordinator (On-site)
Core
Experienced research professional managing day-to-day clinical trial activities, ensuring protocol compliance, data integrity, and operational efficiency while mentoring research staff.
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 management, protocol compliance, data collection and entry, regulatory documentation, staff mentorship, study start-up and close-out, participant screening
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; ensure compliance with GCP and sponsor requirements; collect and enter study data; assist with study start-up, maintenance, and close-out; collaborate with investigators, sponsors, and CROs.
Seniority
Mid-Senior level, hands-on IC
