Travel Clinical Research Coordinator
Core
Utilize Good Clinical Practices (GCP) to screen, enroll, and monitor clinical research study subjects while ensuring protocol and regulatory compliance across decentralized research locations.
Role type
Mid-level Travel Clinical Research Coordinator
Builds
Clinical research studies for sponsors and CROs
Domain
Clinical research / Healthcare
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
ICH/GCP compliance, Good Documentation Practices (GDP), ALCOA-C+ adherence, protocol review, subject recruitment, informed consent administration, adverse event recognition, specimen collection and processing, study medication dispensation, data documentation, regulatory compliance (FDA/ICH)
Preferred skills
Experience with decentralized clinical research processes, ability to work independently with minimal guidance, familiarity with StudyTeam/CRIO databases, training of site staff
Technologies
IVRS/EDC systems, StudyTeam, CRIO
Responsibilities
Review and assess study protocols for feasibility and safety; recruit and screen study subjects; collect and process biological specimens; dispense study medication; document source data and adverse events; train site staff on clinical procedures; coordinate with sponsors and CROs during monitoring visits.
Seniority
Mid-level, hands-on IC
