Clinical Research Associate-Regulatory
Listed on 2026-01-12
-
Healthcare
Clinical Research -
Research/Development
Clinical Research, Research Scientist
Job Objective
Responsible for the development and maintenance of regulatory documents pertaining to the clinical trials conducted by investigators within the Health System. Key to this role is the preparation and maintenance of clinical trial protocols and related regulatory documents for submission to the Eisenhower Human Research Protections Program (Eisenhower Medical Center's Institutional Review Board or IRB) in order to obtain its approval for the clinical trials to proceed.
Acts as a resource to investigators and staff for interpretation and execution of complex clinical research regulations, policies and procedures concerning the conduct of clinical trials, including those of the FDA, OHRP, HHS, Eisenhower IRB, and the Research department. Specialties actively engaged in clinical research include Oncology, HIV, Infectious Disease, Gastroenterology, Cardiology, Orthopedics and Pulmonology.
- Seniority level
Entry level
- Employment type
Full-time
- Job function
Research, Analyst, and Information Technology - Industries Hospitals and Health Care
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