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
Intermediate Clinical Research Coordinator
Builds
Clinical research studies (single site, established procedures, industry sponsorship)
Domain
Healthcare / Clinical Research
Required skills
Participant recruitment and retention, screening for eligibility, study procedures and data collection, specimen handling, adverse event monitoring, protocol implementation, regulatory compliance, stakeholder communication
Preferred skills
ACRP (CCRC/ACRP-CP) or SOCRA (CCRP) certification, knowledge of ICH GCP, IRB, FDA requirements, HIPAA/privacy, CITI certification
Technologies
None stated
Responsibilities
Assist in participant recruitment and screening; perform study procedures and data collection; collect and ship specimens; monitor adverse events and protocol deviations; coordinate study activities and personnel; maintain study binders and filings; distribute study drug materials; assist with protocol amendments; provide orientation to research staff; submit progress reports; support sponsor monitoring visits
Seniority
Intermediate, hands-on IC
