Safety Surveillance Adviser

at  Novo Nordisk

Safety Surveillance Adviser
Category: Reg Affairs & Safety Pharmacovigilance
Location:Søborg, Capital Region of Denmark, DK
Are you passionate about ensuring the safety of pharmaceutical products? Do you have experience in safety surveillance and signal detection?
If you are ready for a new challenge and want to make a difference in the healthcare industry, read on and apply today for a life-changing career!

QUALIFICATIONS

As an ideal candidate, you will have:

• A Master’s degree in Medicine or Natural Sciences (MD, DVM, MSc Pharm or equivalent). PhD is an advantage.
• Experience within pharmacovigilance, and/or within the pharmaceutical industry and a strong desire to specialise within safety surveillance.
• A solid understanding of medical concepts, scientific methodology, and drug development.
• The ability to work independently as well as to collaborate in a continuous developing environment.

Personally, you excel as a strong collaborator in a multicultural, continuously developing environment. You work swiftly in a high-paced environment, consistently meeting timelines. You are self-driven, capable of working independently, and effectively managing pressure when required. Ethical, responsible, well-organized, a team player, and a strong communicator describe your professional attributes.

• Establish the product safety profile during the development and maintenance of the labeling for marketed products.
• Conduct safety surveillance of Novo Nordisk products during pre-approval and post-approval phases, based on safety information from worldwide sources.
• Communicate drug safety issues internally and to health authorities as required.
• Chair or participate in cross-functional safety committees, ensuring effective establishment and execution of meetings.
• Take responsibility for all areas related to patient safety in clinical trials