Clinical Research Coordinator II
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
Builds
Clinical trials for sponsors and CROs
Domain
Healthcare / Clinical Research
Required skills
Clinical trial coordination, patient recruitment and retention, protocol adherence, clinical procedures (vital signs, ECGs, phlebotomy), specimen processing, data management, regulatory compliance (GCP, HIPAA), inventory management
Preferred skills
Experience in gastroenterology, hepatology, or cardiology, CCRC or CCRP certification, CTMS/EDC system proficiency
Technologies
CTMS, EDC systems
Responsibilities
Manage complex study visit schedules and protocol-related activities, lead patient recruitment and retention efforts, conduct protocol-required clinical procedures, process laboratory specimens, maintain accurate study documentation, ensure timely resolution of data queries, prepare for sponsor/CRO/regulatory monitoring visits and audits, review safety reports, maintain inventory of study equipment and investigational products, support process improvement initiatives
Seniority
Mid-Senior, hands-on IC