Clinical Research Coordinator II
Core
Coordinate clinical research studies by screening, enrolling, and monitoring subjects while ensuring protocol and regulatory compliance.
Role type
Clinical Research Coordinator
Builds
Clinical trials for medical research
Domain
Healthcare / Clinical Research
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, phlebotomy, informed consent procedures, adverse event identification, data entry, regulatory document filing, IVRS/EDC systems, MS Office
Preferred skills
Spanish language proficiency, prior Care Access Research experience
Technologies
IVRS, EDC, MS Word, MS Excel
Responsibilities
Screen and enroll study subjects, obtain informed consent, perform clinical procedures (blood draws, vitals, ECGs), review lab/test results, identify and report adverse events, coordinate site visits, maintain source documents and medication inventory, resolve data queries.
Seniority
Mid-level, hands-on IC
