Job Title: (Senior) Safety Surveillance Adviser (1-Year Contract)
Location: Søborg, Denmark
Company: Novo Nordisk
Department: Safety Surveillance, Global Patient Safety
Posted On: February 2025
About the Position:
Novo Nordisk is hiring a (Senior) Safety Surveillance Adviser for a 1-year contract. This position will involve both independent work and collaboration with a highly skilled team across various functional areas, especially the Non-clinical and Clinical Development teams. The primary focus is ensuring the safety of pharmaceutical products throughout their lifecycle, including safety surveillance, communication of safety information, and supporting safety committees.
Key Responsibilities:
Safety Profile Establishment: Develop and maintain the safety profile of products during both development and after market approval.
Safety Surveillance: Monitor Novo Nordisk products’ safety during pre-approval and post-approval phases based on global safety data.
Drug Safety Communication: Communicate safety issues internally and to relevant health authorities.
Support Safety Committees: Assist in organizing and executing safety meetings across functions.
Patient Safety in Clinical Trials: Oversee and ensure patient safety aspects are covered throughout clinical trials.
Qualifications:
Educational Background: Master’s degree in Medicine, Natural Sciences (MD, DVM, MSc Pharm, or equivalent). A PhD/research experience is an advantage but not required.
Experience: Background in pharmacovigilance or clinical development with a strong desire to specialize in safety surveillance.
Skills: Strong understanding of medical concepts, scientific methodology, and drug development processes. Excellent communication skills in English (both written and spoken).
Personal Traits: A self-driven team player who thrives in a multicultural and evolving environment, with strong organizational and collaboration skills. Able to work independently, handle pressure, and meet tight deadlines.
About the Department:
The Safety Surveillance department within Global Patient Safety is responsible for the monitoring and management of all safety information related to Novo Nordisk’s products, whether they are marketed or still in development. The department also handles safety updates, risk management plans, and aggregate reports, fostering a collaborative and positive team culture.
Working at Novo Nordisk:
Novo Nordisk is committed to making a difference in the healthcare industry by embracing change and innovation. The company values collaboration, adaptability, and development opportunities, creating a dynamic environment for employees to thrive and contribute to meaningful patient care.
How to Apply:
Deadline: March 7, 2025
Please submit your application as soon as possible, as applications are reviewed on an ongoing basis. Include a brief statement about why you are applying in your resume or CV (no cover letter required). Avoid adding a photo to your CV to ensure an efficient recruitment process.
Contact:
For more information, please contact Senior Director Brian Sonne Stage at oisg@novonordisk.com.
Important Notes:
Novo Nordisk is committed to an inclusive recruitment process and equal opportunities for all candidates.
The company embraces diversity and works toward creating an inclusive culture for employees, patients, and communities.
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