Join the Office of Research, a regional center for high quality clinical research, as the experienced and multi-faceted team works to provide key assistance in a broad range of clinical trials to meet the needs of the community. The team is seeking a professional, self-confident, and organized individual to perform a variety of subject care and administrative duties. This role provides direct supervision to clinical research nurses, clinical research coordinators and data specialists, as well as coordinates and participates in clinical research studies conducted by physicians.
Supervisory responsibilities include monitoring study visits to ensure proper protocol is met, providing timely feedback to staff, and attending leadership training.
Clinical research coordinator responsibilities include reviewing institutional review board protocol, coordinating study initiation, screening potential participants, and collecting accurate patient data in compliance with Good Clinical Practice.
SHIFT: Monday - Friday, 8AM to 4PM. Hours slightly flexible. No weekends.
Required Skills
Required Experience