Senior Safety Surveillance Professional

2 days ago


Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full time

At Novo Nordisk A/S, we are seeking a skilled Safety Surveillance Specialist to join our team.

About the Position

You will be responsible for establishing and maintaining product safety profiles during development and post-approval phases. This includes conducting safety surveillance of Novo Nordisk products based on worldwide safety information sources.

  • Establishing and maintaining the product safety profile during development and post-approval phases.

  • Conducting safety surveillance of Novo Nordisk products during pre-approval and post-approval phases, based on safety information from worldwide sources.

  • Communicating drug safety issues internally and to health authorities as required.

  • Chairing or participating in cross-functional safety committees, ensuring effective establishment and execution of meetings.

  • Taking responsibility for all areas related to patient safety in clinical trials.

Requirements

To succeed in this role, you must have:

  • A master's degree within Medicine or Natural Sciences (MD, DVM, MSc Pharm or equivalent), complemented by a PhD/research experience.
  • Several years of experience within pharmacovigilance and a strong desire to specialize within safety surveillance.
  • A solid understanding of medical concepts, scientific methodology, and drug development.
  • Excellent communication skills, both written and spoken, with fluency in English.

You should be a team player who thrives in a multicultural and continuously evolving environment. You should also be self-driven and capable of working independently, handling pressure, and meeting tight deadlines in a fast-paced setting.



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