#NMDPharma is #hiring!
We’re looking for a Regulatory Writer based in Denmark (Aarhus or Copenhagen), the USA (East Coast), or remotely based in Europe. If you have experience in producing regulatory documents for health authority submissions, we’d love to hear from you.
As a growing #biotech with three ongoing Phase 2 trials, we are expanding our Regulatory team and therefore looking for a Regulatory Writer on location or remote (full-time or part-time). Key responsibilities include producing investigator brochures, health authority meeting packages/briefing books, annual reports, and other key clinical and regulatory documents.
Find out more about this exciting opportunity and apply online through the link below: https://lnkd.in/dnSjNcfE
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