Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, is seeking a Manager of Regulatory Affairs to oversee regulatory operations for site clinical operations. You will develop and implement strategies to ensure FDA compliance and manage audits, while guiding the regulatory team and coordinating with sponsors and investigators.
The role requires a Bachelor's degree, knowledge of FDA and GCP guidelines, and at least three years of regulatory experience (including supervisory
#J-18808-LjbffrRegulatory Affairs Manager – Oncology Clinical Trials in nashville at Unknown Company
This position is listed as full time and onsite.