Associate Director Pharmaceutical Affairs Benelux

beonemedicines.sg

Belgium
**
Qualified person responsible for information and publicity
Local contact person for pharmacovigilance
Prevention advisor
** BeOne Medicines is seeking an Associate Director of Pharmaceutical Affairs for its operations in Belgium and Luxembourg. The ideal candidate will be responsible for regulatory compliance, medical information, and pharmacovigilance while working collaboratively across departments to support the fight against cancer. **

Job Summary

  • The Associate Director Pharmaceutical Affairs acts as the Qualified Person Responsible for Information and Publicity (QP RIP) and is responsible for medical information and publicity in Belgium and Luxembourg.
  • This role steers locally the quality, regulatory and compliance activities within the affiliate and in collaboration with EU departments in accordance with Belgian, Dutch and Luxembourg laws and regulations.
  • The position also fulfills the role of the Prevention advisor, provides ad hoc PMO, and endorses transversal activities carried out by various EU and BeLux departments.

Matching Summary

Match Score: 75

** BeOne Medicines is seeking an Associate Director of Pharmaceutical Affairs for its operations in Belgium and Luxembourg. The ideal candidate will be responsible for regulatory compliance, medical information, and pharmacovigilance while working collaboratively across departments to support the fight against cancer. **

Skills & Requirements

Must-have

  • Qualified Person Responsible for Information and Publicity
  • Local contact Person for Pharmacovigilance
  • Prevention Advisor
  • regulatory affairs in Belgium
  • medical information management
  • promotional and medical material review

Nice-to-have

  • scientific and business professionals
  • highly motivated, collaborative
  • passionate interest in fighting cancer
  • working in a dynamic, lean environment
  • cross-functional collaboration
  • out-of-the-box thinking

Key Requirements

  • Minimum of 10 years pharmaceutical industry/biotech experience
  • Certified Prevention Adviser Level III
  • Fluent in English, French or Dutch
  • Oncology market experience
  • PharmD or PhD, or Bachelor/Master of Science

Work Rights

Not specified

Tailored Resume

Cover Letter