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 data and patient outcomes
Domain
Clinical research / Healthcare
Required skills
Clinical trial management, patient recruitment and retention, regulatory compliance (GCP/FDA), clinical procedures (vital signs, ECGs, phlebotomy), data management (CTMS/EDC), staff mentorship, inventory control, safety reporting
Preferred skills
CCRC or CCRP certification, experience mentoring junior staff
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; maintain study inventory.
Seniority
Senior, hands-on IC