The primary purpose of this position is to recruit and retain study subjects while coordinating their visits and managing data gathered as a result of their investigator participation, initiated, and sponsored research projects, all while staying compliant with FDA and IRB guidelines and regulations. This position also involves a laboratory aspect. Sample retrieving, processing, and shipping for investigator-led and sponsored studies. The division's primary biorepository management while maintaining other laboratory functions and safety. Monitor compliance with study procedures with Federal, State, and University regulations. Ensures that documents such as eligibility forms and informed consent are appropriately gathered and maintained, HIPAA regulations are followed, and that infection control and safety procedures are implemented. Prepares and maintains regulatory and compliance documents such as IRB applications. Collects and analyzes data from clinical trials or other medical screenings. This position is grant funded.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed