Senior Pharmacovigilance Expert in Rare Diseases

1 day ago


Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full time
About the Role

We are seeking an experienced Senior Pharmacovigilance Expert to join our Safety Surveillance Rare Disease team at Novo Nordisk. As a key member of our global safety function, you will be responsible for leading and driving safety surveillance activities in development projects for rare diseases.

Key Responsibilities
  • Chair cross-functional drug safety committees to ensure seamless collaboration across teams.
  • Prepare and communicate benefit-risk assessments to stakeholders, showcasing your exceptional communication skills.
  • Contribute to the development of clinical study designs and protocols, leveraging your expertise in pharmacovigilance.
  • Communicate effectively with external parties related to clinical safety monitoring, such as Data Monitoring Committees.
  • Represent Safety Surveillance in cross-functional teams, providing guidance and support as needed.
Qualifications and Requirements
  • Several years of experience in Safety Surveillance and development in the pharmaceutical industry.
  • A master's degree in Medicine or Natural Sciences, complemented by a PhD/research experience or equivalent.
  • Interest/experience in data analysis and analysis tools (e.g., JMP and/or Qlik Sense).
  • Experience with rare diseases, hemophilia, or hemoglobinopathies is an advantage.
  • The ability to work independently and collaboratively in a dynamic environment.
  • Good communication skills and the ability to establish contacts with stakeholders within and outside the organization.
About Novo Nordisk

At Novo Nordisk, we're committed to creating an inclusive culture that celebrates diversity, promotes equality, and fosters innovation. We believe that talented employees with diverse perspectives and backgrounds are essential to our success. Join us on our mission to drive change and improve patient care.



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