Medical Doctor within Pharmacovigilance

Category: Reg Affairs & Safety Pharmacovigilance

Location:Søborg, Capital Region of Denmark, DK

• Bringing a broad and in-depth understanding of medical concepts, disease processes, and therapeutic areas when assessing the potential risk to patients in relation to product quality issues, and potential recall situations.
• Being a medical expert when interacting with internal and external stakeholders, cross-functional areas in HQ, affiliates, and health authorities.
• Reviewing clinical trial and non-interventional study protocols to ensure adequate collection of relevant safety information according to regulatory requirements and Novo Nordisk procedures.
• Chairing “Cross Functional Groups” in clinical trials within Global Safety.

• A Medical Doctor degree.
• Experience within pharmacovigilance or clinical experience with a strong urge to specialize in pharmacovigilance.
• In-depth understanding of diagnostic processes, diagnostic techniques, and interpretation of diagnostic results.
• The ability to evaluate the impact and consequences of diseases and medical interventions.
• An excellent communication skills and proficiency in English both written and spoken.