Medical Writer - Triptane
(m/f/d)
Freelance/Contracting project Baden-Wurttemberg Start date: asap Reference number: 836319/1
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Responsibilities
1. Drafting and revising regulatory documents in accordance with EU requirements (, CTD Modules and
2. Ensuring compliance with regulatory standards and guidelines (, EMA, ICH)
3. Collaborating with internal teams to align on content and timelines
4. Supporting strategic planning and execution of the dossier update
Profile
5. Proven experience as a Medical Writer in a regulatory setting, preferably with a focus on migraine therapeutics
6. Familiarity with European regulatory documentation requirements
7. Knowledge of triptans or other migraine-related active substances
8. Excellent written and spoken English skills
9. Independent, structured, and reliable working style
Benefits
10. Remote work possible