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Novo Nordisk

Regulatory Affairs Professional, RA Diabetes, CV, Liver and Rare Disease

Søborg, Capital Region of DenmarkDKK570K - DKK838K / yearPosted 1 weeks ago
Full-timeonsitemid

Job Description

  • Contribute with regulatory expertise to global strategies and tactics
  • Develop regulatory documentation for submission to Health Authorities globally, e.g. clinical trial applications, briefing packages, paediatric plans, and responses to health authority questions
  • Represent Regulatory Affairs in global clinical trial teams and other cross-functional teams
  • Collaborate effectively with cross-functional stakeholders such as project managers, medical and non-medical specialists, statisticians, and medical writers
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    Pharmaceuticals
    10001+ employees
    Bagsværd, DK
    Website
    Regulatory Affairs Professional, RA Diabetes, CV, Liver and Rare Disease at Novo Nordisk | Renata