Clinical Research Coordinator - Future Opportunities
Core
Independently coordinate and manage industry-sponsored clinical trials from study start-up through closeout, ensuring compliance with protocol requirements, regulatory standards, and patient safety guidelines.
Role type
Senior IC Clinical Research Coordinator (CRC II)
Builds
Clinical trials in gastrointestinal, hepatology, obesity, and cardiology
Domain
Clinical research / Healthcare
Required skills
Clinical trial coordination, patient recruitment and retention, protocol adherence, GCP compliance, clinical procedures (vital signs, ECGs, phlebotomy), specimen processing, data management (CTMS, EDC), regulatory documentation, safety reporting, inventory management
Preferred skills
Therapeutic area experience (gastroenterology, hepatology, cardiology), CCRC or CCRP certification, CTMS/EDC proficiency
Technologies
CTMS, EDC systems
Responsibilities
Manage complex study visit schedules and protocol-related activities; Lead patient recruitment and retention efforts; Conduct protocol-required patient visits and assessments; Process laboratory specimens and prepare shipments; Maintain accurate study documentation and resolve data queries; Serve as primary point of contact for study participants; Prepare for sponsor, CRO, and regulatory monitoring visits; Review safety reports; Maintain inventory of study equipment and investigational products; Support process improvement initiatives
Seniority
Mid-level, hands-on IC