Clinical Research Coordinator 2
Core
Mid-level clinical research professional assisting in planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies from initiation to close-out.
Role type
Mid-level Clinical Research Coordinator
Builds
Clinical research studies
Domain
Healthcare / Clinical Research
Deliverable
physical/clinical work
Required skills
Protocol implementation, participant recruitment and screening, specimen handling, adverse event monitoring, regulatory compliance, study drug distribution, protocol amendment support, study orientation, progress reporting, administrative coordination
Preferred skills
Cultural competency, health literacy support, language translation strategies
Technologies
Office software, relevant computer applications
Responsibilities
Assist in participant recruitment and eligibility screening; Perform study procedures and data collection for moderate risk protocols; Collect, process, pack, and ship specimens; Maintain study binders and filings; Distribute study drug materials; Monitor and report adverse events and protocol deviations; Assist in implementing protocol amendments; Assist with study orientation and in-services; Monitor protocol implementation and submit progress reports; Coordinate communications with sponsors and regulatory bodies; Manage administrative tasks for study personnel
Seniority
Mid-level, hands-on IC
