Associate Director, PV Regulatory Intelligence
Provide Global Regulatory Intelligence for Clinical and Post approval Pharmacovigilance for LCS and LCS Customers.
Responsibilities
Minimum Required Education and Experience
5-7 years of relevant Pharmacovigilance experience
At least 3 years of experience with assessing global PV Regulatory Intelligence
5 years in Lifecycle Safety (e. g. , Pharmacovigilance, CEVA, Medical Info, Safety Publishing, Risk Management)
Equivalent combinations of education, training, or experience accepted
Practical knowledge of Global PV Regulations
Skills and Abilities
- solving
This role is not available for a UK visa sponsorship.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
- Informații detaliate despre oferta de muncă
Firma: IQVIA Localiția: Bucureşti
Bucharest, Bucharest, RomaniaAdăugat: 13. 9. 2025
Postul de muncă activ
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