Clin/Tran Research Coord II
Core
Coordinates approval processes and conduct of clinical/translational research protocols to maintain integrity and quality.
Role type
Clinical Research Coordinator II
Builds
Clinical trials and research studies
Domain
Healthcare / Clinical Research
Required skills
IRB proposal preparation, regulatory compliance, study budget management, human subject advocacy, informed consent process, data recording on case report forms, specimen shipping, participant screening and recruitment
Preferred skills
Qualitative and quantitative research methods, project coordination, networking (via careerplan.io/jobs/R-68571-1-clintran-research-coord-ii-at-vumc)
Technologies
Electronic case report forms, project management repositories
Responsibilities
Prepare and process IRB research proposals, amendments, and continuing review applications; maintain regulatory documents for sponsor and authority review; procure equipment and supplies; screen and recruit eligible study participants; record data from source documentation to case report forms; package and ship study specimens; manage study budgets and billing compliance; participate in the informed consent process; attend research staff council meetings.