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 (II)
Builds
Clinical trials for medical breakthroughs and community health access
Domain
Clinical research / Healthcare
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GCP knowledge, FDA/ICH guideline adherence, adverse event identification, informed consent procedures, data entry, patient recruitment, phlebotomy, vital signs/ECG collection, regulatory document filing
Preferred skills
Care Access Research experience, independent operation, stakeholder communication
Technologies
Clinical trials database, IVR systems, electronic data capture (EDC), MS Word, 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 coordinators; recruit patients; maintain regulatory documentation
Seniority
Senior, hands-on IC