Independent in the preparation of IRB protocols, consent forms, and development of study
Completes and maintains all study documents as required.
Actively works to identify and recruit study
Ensures proper research billing in EPIC.
Work as a team player with all involved in the studies.
Scheduled Days / Hours: M-F
Bachelors Degree preferred.
Minimum 3-5 years of clinical research experience required.
MA, LPN, Phlebotomy or CRCC preferred.