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 (moderate risk protocols)
Domain
Healthcare / Clinical Research
Required skills
Participant recruitment and screening, study procedure execution, data collection and recording, specimen handling and shipping, adverse event monitoring and reporting, protocol amendment implementation, regulatory compliance adherence, study binder maintenance, drug distribution, study progress reporting, administrative coordination
Preferred skills
Cultural competency, language translation support, health literacy adaptation
Technologies
None stated
Responsibilities
Assist in participant recruitment and eligibility screening; Perform study procedures and daily operations of moderate risk protocols; Collect, process, pack, and ship specimens; Monitor and report adverse events and protocol deviations; Assist in implementing protocol amendments; Maintain study binders and filings; Distribute study drug materials; Monitor study progress and submit reports; Assist with study orientation and in-services; Adhere to regulatory and university policies