Clinical Research Coordinator II
Core
Coordinate screening, enrollment, and monitoring of 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
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Good Clinical Practices (GCP) knowledge, FDA/ICH guideline adherence, adverse event identification, informed consent administration, basic clinical procedures (phlebotomy, vitals, ECGs), data entry and query resolution, patient recruitment, regulatory document filing
Preferred skills
Prior Care Access experience, phlebotomy certification, independent operation
Technologies
Clinical trials databases, IVR systems, electronic data capture (EDC), MS Word, MS Excel
Responsibilities
Screen and enroll study participants; obtain informed consent; perform basic clinical procedures; monitor patient compliance and adverse events; enter data in real-time; coordinate site visits; mentor junior coordinators; assist with recruitment planning
Seniority
Senior, hands-on IC
