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Senior Safety Surveillance Adviser

0-2 years
Not Disclosed
10 Feb. 24, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Senior Safety Surveillance Adviser
Location: Søborg, Denmark
Company: Novo Nordisk
Department: Safety Surveillance, Global Patient Safety
Posted On: February 2025

About the Position:

Novo Nordisk is looking for a Senior Safety Surveillance Adviser to join their Safety Surveillance team, responsible for monitoring the safety of pharmaceutical products. This position involves both independent and collaborative work with internal teams across multiple functions. You will play a key role in ensuring patient safety through pre-approval and post-approval safety surveillance, as well as contributing to the development of safety profiles and drug labelling.

Key Responsibilities:

  • Safety Surveillance: Monitor the safety of Novo Nordisk products during pre-approval and post-approval phases, utilizing global safety data.

  • Drug Safety Communication: Report safety information and drug safety concerns internally and to health authorities.

  • Cross-Functional Collaboration: Chair or participate in safety committees, ensuring the effectiveness of meetings and execution of safety initiatives.

  • Clinical Trials Oversight: Take responsibility for patient safety aspects during clinical trials, ensuring compliance and safety.

Qualifications:

  • Educational Background: Master's degree in Medicine, Natural Sciences (e.g., MD, DVM, MSc Pharm), or equivalent. A PhD or research experience is an advantage but not required.

  • Experience: Several years of experience in pharmacovigilance with a focus on safety surveillance.

  • Skills: Strong knowledge of medical concepts, drug development, and scientific methodologies. Excellent communication skills in both written and spoken English.

  • Personal Traits: Self-driven, collaborative, organized, and adaptable with the ability to handle pressure and meet deadlines in a fast-paced environment.

About the Department:

The Safety Surveillance department is part of Global Patient Safety and is responsible for monitoring safety information across all Novo Nordisk products, whether they are marketed or under development. The department manages safety updates, risk management plans, and aggregate reports. The team fosters a positive, inclusive, and collaborative work culture.

Working at Novo Nordisk:

Novo Nordisk is committed to driving change in the healthcare industry, focusing on patient care and striving for excellence. The company values experimentation, growth, and adaptation, creating a dynamic environment where employees can thrive and make a meaningful impact.

How to Apply:

Deadline: March 7, 2025
Please submit your application early, as applications will be reviewed on an ongoing basis. Include a brief statement in your CV about why you're applying for the role (no cover letter required). Avoid adding a photo to your CV for an efficient recruitment process.

Contact:
For more information, please contact Senior Director Brian Sonne Stage via email at oisg@novonordisk.com.

Important Notes:

  • Novo Nordisk is committed to an inclusive recruitment process, providing equal opportunities for all candidates.

  • The company encourages diverse perspectives, backgrounds, and cultures, both within the company and the communities they serve.