Senior Cardiovascular Safety Surveillance Lead

Novo Nordisk

Gladsaxe Kommune

On-site

DKK 743,000 - 1,092,000

Full time

4 days ago
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Job summary

Novo Nordisk in Søborg, Denmark, seeks a Safety Surveillance Specialist to shape the safety profile of assets in clinical development. You will lead analytical and medical evaluation of emerging safety data and translate findings into clear insights guiding project decisions.

The role emphasizes collaboration with Clinical Development, Regulatory Affairs, Biostatistics and external partners, supporting growth through mentorship and adaptability.

Qualifications

  • Master’s degree in Medicine or Natural Sciences (e.g., MD, DVM, MSc Pharm or equivalent).
  • Experience in drug development, clinical safety or pharmacovigilance.
  • Solid understanding of drug development, regulatory requirements and GxP.

Responsibilities

  • Lead analytical and medical evaluation of emerging aggregate safety data.
  • Drive safety assessments and benefit‑risk evaluations across development programmes.
  • Prepare safety contributions to study reports, regulatory submissions, and protocols.
  • Represent Safety Surveillance in cross‑functional teams and external meetings.
  • Identify and drive initiatives strengthening scientific and strategic excellence.
  • Contribute to a collaborative, inclusive team environment.

Skills

Analytical thinking
Communication
Mentorship
Team collaboration
Independent work
Adaptability
Stakeholder management

Education

Master’s degree in Medicine or Natural Sciences

Job description

Novo Nordisk in Søborg, Denmark, seeks a Safety Surveillance Specialist to shape the safety profile of assets in clinical development. You will lead analytical and medical evaluation of emerging safety data and translate findings into clear insights guiding project decisions.

The role emphasizes collaboration with Clinical Development, Regulatory Affairs, Biostatistics and external partners, supporting growth through mentorship and adaptability.

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