Associate Director, Pharmacovigilance Vendor Management
On-site · Hellerup, Region Hovedstaden, Kingdom of Denmark
Job Summary
Associate Director, Pharmacovigilance Vendor Management responsible for leading PV activities across Organized Data Collection programs for marketed products, structuring PV processes globally, overseeing vendor performance and CAPA, and collaborating across GVP Compliance, Commercial, Medical Affairs, and affiliates. The role requires expertise in FDA safety regulations, ICH/GVP guidelines, and global PV regulations, with a track record in vendor oversight, PV training, and crisis management initiatives. Travel up to 20 days/year; based in Hellerup, Denmark.
Required Qualifications
- Bachelor’s degree in a health-related discipline (preferably)
- minimum 8 years of Pharmacovigilance experience
- Expert knowledge of FDA safety regulations, ICH Guidelines, GVP requirements, and applicable global pharmacovigilance regulations and guidance
- Experience in cross-functional, matrixed environments
- Strong communication and collaboration skills
- Travel: 10-20 days per year
- Office: Tuborg Boulevard 12, 2900 Hellerup, Denmark
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