Clinical Research Study Coordinators in the East Carolina Diabetes & Obesity Institute (ECDOI) are responsible for assisting Principal Investigators (PI) in ECDOI in the planning, subject recruitment, testing, study execution, and data collection and analysis of human clinical and translational research studies.
Specific duties and responsibilities include, but may not be limited to, the following:
coordinating with PIs project objectives, needs and study coordinator percent effort requirements,
coordinating organization and protocol development,
working directly with collaborating laboratory personnel (if applicable),
developing IRB protocols, applications and amendments,
developing standard operating procedure manuals for approval from funding agencies,
submission of progress reports to funding agencies
development/organization of database systems (e.g., REDCap)
ensuring compliance with recruiting, evaluating, and instructing clinical research volunteers including all facets of informed consent,
ensuring compliance with all HIPPA regulations
ensuring safe proper execution of all experimental protocols
collection/oversight of tissue and/or blood sample collection, processing and analysis,
data collection, proper entry into data bases, analysis and interpretation,
assisting in the dissemination of research findings,
coordinating percent effort distribution among different projects.
B.S. in biological sciences or related field.
Research Project Experience.