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Director, Medical Writing
- Permanent
- Medical Communications, Medical Writing, Media & Publishing
- United States
- Experience in regulatory medical writing within the biotech or pharmaceutical industry.
- Demonstrated expertise in authoring regulatory submissions (e.g., NDAs, INDs, etc.).
- Strong understanding of regulatory guidelines (e.g., FDA, EMA, ICH).
- Exceptional communication and collaboration skills.
- Market-beating base salary and a competitive bonus structure.
- Significant stock equity.
- 100% company-paid medical, dental, and vision coverage for employees.
- Generous Paid Time Off (PTO) and retirement plan.
If you are having difficulty in applying or if you have any questions, please contact George Watson at g.watson@proclinical.com
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