Senior Clinical Research Coordinator
Core
Lead and independently manage complex industry-sponsored clinical trials from study start-up through closeout, overseeing patient recruitment, regulatory compliance, and site operations.
Role type
Senior Clinical Research Coordinator (hands-on IC)
Builds
Clinical trial execution and patient enrollment for sponsors in GI, hepatology, obesity, and cardiology
Domain
Clinical Research / Healthcare
Required skills
Clinical trial management, patient recruitment and retention, GCP compliance, protocol adherence, data management, staff mentorship, clinical procedures (vital signs, ECGs, phlebotomy), regulatory reporting, inventory management
Preferred skills
CCRC or CCRP certification, experience mentoring junior staff, process improvement
Technologies
CTMS, EDC systems
Responsibilities
Lead complex clinical trials from start-up to closeout; coordinate study visits and ensure regulatory compliance; lead patient recruitment and retention; mentor junior coordinators; perform clinical procedures including vital signs, ECGs, and specimen collection; process and ship laboratory specimens; maintain study documentation and resolve data queries; serve as primary contact for sponsors and investigators; prepare for monitoring visits and audits; review safety reports; manage study inventory and supplies.
Seniority
Senior, hands-on IC