Clinical Translational Research Coordinator II - Onsite, Nashville TN
Core
Coordinates approval processes and conduct of clinical/translational research protocols to maintain integrity and quality.
Role type
Clinical Translational Research Coordinator
Builds
Clinical trials and research studies
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
IRB proposal preparation, participant recruitment and screening, case report form data entry, specimen shipping, study budget management, informed consent process, regulatory compliance documentation
Preferred skills
Oncology experience, patient interaction, independent work, multi-site coordination
Technologies
Electronic case report forms, shipping guidelines
Responsibilities
Prepare and process IRB research proposals, amendments, and adverse event reports; recruit and screen eligible participants; record data from source documentation to case report forms; package and ship study specimens; manage study budgets and billing compliance; participate in informed consent processes; maintain regulatory documentation for sponsor and authority reviews.