Job Summary
A company is looking for a Consultant to join their Regulatory Affairs team.
Key Responsibilities
- Provide ad-hoc regulatory guidance across critical therapeutic areas
- Navigate complex regulatory landscapes for specified therapeutic areas
- Consult in domain areas to enhance service offerings and contribute to clinical trials
Required Qualifications
- Minimum BS degree in a science-related field
- 3+ years as a Regulatory Project Manager or equivalent in the clinical research industry
- Prior experience working directly for the FDA
- Expertise in Neuroscience, Pediatrics, Rare Disease, or Women's Health
- Advanced knowledge of US and International regulatory requirements
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