Job Summary
A company is looking for a Senior Manager & Editor FDA Submissions.
Key Responsibilities
- Ensure timely delivery of consistent, high-quality, accurate and complete written materials
- Write and edit large-scale FDA submission documents, effectively integrating science and advocacy
- Manage internal stakeholder relationships and supervise contract resources as needed
Required Qualifications
- Bachelor's or Advanced Degree in a regulatory, law, science or related field; advanced degree preferred
- 10+ years of relevant experience writing or editing business, public affairs, regulatory or legal documents
- Understanding of FDA processes and experience developing FDA submissions preferred
- Demonstrated ability to synthesize complex information using excellent critical thinking skills
- Demonstrated success in engagement and collaboration skills across diverse stakeholder groups
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