Clinical Research Coordinator I
Core
Screen, enroll, and monitor clinical research study subjects while ensuring protocol and regulatory compliance.
Role type
Junior Clinical Research Coordinator (IC)
Builds
Clinical trials for medical breakthroughs and community health access
Domain
Clinical Research / Healthcare
Deliverable
client delivery
Required skills
GCP knowledge, patient screening, informed consent, vital signs/ECG/blood draws, adverse event reporting, data entry, regulatory documentation, study medication management, patient recruitment support
Preferred skills
Phlebotomy experience, familiarity with clinical trial databases/IVR/EDC, ability to work with minimal supervision
Technologies
Clinical trials database, IVR systems, EDC, MS Word, MS Excel
Responsibilities
Prescreen study candidates and obtain informed consent; Complete basic clinical procedures (blood draws, vital signs, ECGs); Review lab results and test data for completeness; Identify and report adverse events; Record data in real-time and resolve queries; Assist with patient recruitment and site visit coordination
Seniority
Junior, supervised IC
