Clinical Research Coordinator I
Core
Coordinate screening, enrollment, and monitoring of clinical research study subjects while ensuring protocol and regulatory compliance.
Role type
Junior Clinical Research Coordinator (IC)
Builds
Clinical trial data and patient care processes for global health research programs
Domain
Clinical Research / Healthcare
Deliverable
client delivery
Required skills
GCP knowledge, patient recruitment, data entry, adverse event reporting, regulatory compliance documentation, phlebotomy, vital signs/ECG collection, study medication management
Preferred skills
Bachelor's degree, clinical trial database experience, IVRS/EDC proficiency, MS Office skills
Technologies
Clinical trials database, IVRS, EDC, MS Word, MS Excel
Responsibilities
Prescreen study candidates and obtain informed consent; Complete visit procedures and basic clinical procedures (blood draws, vitals, ECGs); Review lab results and test data for completeness; Identify and report adverse events; Record data in real-time and resolve data queries; Coordinate site visits with sponsors/CROs; Assist in patient recruitment planning.
Seniority
Junior, supervised IC