Regulatory Affairs Intern
2 weeks ago
Work with clinical study teams to ensure appropriate regulatory support from CROs and other partners.
- Serve as additional resource to regulatory teams to track changes in EU and UK legislation and guidelines thereby ensuring Regeneron remains compliant with same.
- Ensure agency correspondence is filed and archived in accordance with Regeneron’s processes.
- Support agency interactions such as scientific advice, national meetings etc.
- Support members of the regulatory team including Regulatory Submission Project Management (RSPM) with any emerging regulatory projects, workstreams, processes or work instructions.
**Skills required**:
- Currently studying for a Degree in life sciences
- Some knowledge of clinical trial and associated regulatory processes preferable but not essential
- Strong Technical writing and oral communication skills essential
- Ability to work in cross functional teams
- Strong attention to detail and adherence to deadlines
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