Clinical Research Coordinator II
Core
Utilize Good Clinical Practices (GCP) to screen, enroll, and monitor clinical research study subjects while ensuring protocol and regulatory compliance.
Role type
Senior Clinical Research Coordinator (IC)
Builds
Clinical trials for diverse health research programs
Domain
Clinical research / Healthcare
Required skills
GCP knowledge, FDA/ICH guideline adherence, patient recruitment, informed consent, adverse event reporting, data documentation, phlebotomy, vital signs/ECG collection, regulatory document filing
Preferred skills
Bachelor's degree, 3+ years CRC experience, Care Access experience, independent operation, stakeholder management
Technologies
Clinical trials database, IVR systems, electronic data capture (EDC), MS Word, MS Excel
Responsibilities
Screen and enroll study subjects; obtain informed consent; perform basic clinical procedures (blood draws, vitals, ECGs); monitor quality metrics and resolve queries; identify and report adverse events; coordinate site visits; mentor junior CRCs; recruit patients; document data in real-time.
Seniority
Senior, hands-on IC