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About the Role:
- High-impact regulatory role enabling patient access to life-saving treatments outside clinical trials.
- Focus on ensuring full regulatory and pharmacovigilance compliance across multiple countries.
- Collaborate with Medical Affairs, Quality, Supply Chain, and external biopharma partners.
Key Responsibilities:
- Support development and execution of regulatory strategies for Expanded Access Programs.
- Prepare and submit regulatory dossiers for cohort and named-patient programs.
- Liaise with pharmacovigilance vendors for global safety reporting.
What We Offer:
- Fully remote international working environment.
- Meaningful, mission-driven work improving access to potentially life-saving treatments.
- Strong career development opportunities within a fast-growing global organization.
Jobgether
Jobgether uses AI-powered matching to connect candidates with jobs at partner companies. They are a fast-growing global organization with a dynamic scale-up environment and high autonomy.