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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
Job Category: Reg Affairs & Safety Pharmacovigilance


Job Description

We are looking for a Senior Safety Surveillance Adviser to join Novo Nordisk. If you have experience in safety surveillance and signal detection, and are passionate about ensuring the safety of pharmaceutical products, this could be the perfect role for you. As part of a dynamic team, you will have the opportunity to work independently and collaborate with colleagues from various functional areas.


Key Responsibilities

  • Establish the product safety profile during development and manage labelling for marketed products.

  • Conduct safety surveillance for Novo Nordisk products in both pre-approval and post-approval phases based on global safety data.

  • Communicate drug safety issues internally and to health authorities.

  • Lead or participate in cross-functional safety committees, ensuring effective meeting execution.

  • Oversee patient safety in clinical trials.


Qualifications

To succeed in this role, we expect you to have:

  • A Master’s degree in Medicine or Natural Sciences (MD, DVM, MSc Pharm, or equivalent). A PhD or research experience is preferred.

  • Several years of experience in pharmacovigilance and a strong desire to specialize in 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 with the ability to work independently in a fast-paced environment.

  • Capable of managing pressure and meeting tight deadlines.

  • Ethical, responsible, and adaptable in a multicultural setting.


About the Department

The Safety Surveillance CagriSema team within Global Patient Safety at Novo Nordisk is responsible for establishing the product safety profile during clinical development. The team works closely with the Non-clinical and Clinical Development teams to evaluate emerging safety data for compounds related to obesity and type 2 diabetes.


Working at Novo Nordisk

At Novo Nordisk, we drive change and embrace experimentation to improve patient care. We work across research, development, manufacturing, marketing, and sales, striving to make a difference.