Regulatory Affairs Manager _ MIND Center Clinical Research
University of Mississippi Medical Center(29 days ago)
About this role
The Regulatory Affairs Manager for the MIND Center Clinical Research program oversees regulatory documentation review and provides institutional guidance on regulatory requirements for clinical research. The role centralizes training and interpretation of requirements from local and external IRBs, sponsors, and regulatory agencies to ensure compliance with UMMC, FDA, and ICH standards. The position operates within a central research service office supporting clinical trial activities across the institution.
Required Skills
- Analytical
- Regulatory Compliance
- GCP
- FDA Regulations
- ICH Guidelines
- HIPAA
- Project Management
- Training
- IRB Submissions
- SOP Development
+2 more
Qualifications
- Bachelor's Degree
- Master's Degree (Preferred)
- CCRP (Preferred)
- CRA (Preferred)
About University of Mississippi Medical Center
umc.eduUMMC educates health care professionals, conducts health sciences research, provides leading patient care and eliminates health care disparities.
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