Clinical Research Coordinator II (Relocation Opportunity)
Core
Coordinate screening, enrollment, and monitoring of clinical research study subjects while ensuring protocol and regulatory compliance.
Role type
Mid-level Clinical Research Coordinator (IC)
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, adverse event identification, informed consent procedures, data entry and management, patient recruitment, phlebotomy, vital signs and ECG collection, regulatory document filing
Preferred skills
Prior experience at Care Access Research, recent phlebotomy certification
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 (blood draws, vitals, ECGs), monitor patient compliance and resolve data queries, identify and report adverse events, coordinate site visits with investigators and sponsors, mentor junior coordinators, assist in recruitment planning
Seniority
Mid-level, hands-on IC