Senior Clinical Research Coordinator
Core
Coordinate clinical trial processes from initiation to close-out, ensuring patient safety, regulatory compliance, and data accuracy for oncology research studies.
Role type
Senior Clinical Research Coordinator (IC)
Builds
Clinical trial execution and patient care activities
Domain
Healthcare / Clinical Research / Oncology
Required skills
Clinical trial protocol execution, patient recruitment and enrollment, regulatory compliance (GCP/FDA/ICH), data abstraction and documentation, adverse event reporting, specimen collection and processing, informed consent management, study feasibility assessment, IRB submission support, research staff mentorship
Preferred skills
Registered Nurse (R.N.) licensure, SOCRA or ACRP certification, phlebotomy skills
Technologies
Case report forms, clinical research databases, study management systems
Responsibilities
Coordinate patient screening, enrollment, and follow-up visits; collect and process study specimens; document adverse events and protocol deviations; prepare regulatory submissions and IRB documents; support sponsor monitoring and audit activities; train and mentor research staff
Seniority
Senior, hands-on IC