Senior Pharmacovigilance Licensing Manager

Seeking a Senior PV Licensing Manager with responsibility to manage the end-to-end process of developing and implementing Pharmacovigilance agreements.

Key Responsibilities

• Collaborating with partners that delivers compliance and efficiency for both parties.
• Collaborate with Global functions providing advice and support for commercial agreements.
• Oversee and manage pharmacovigilance collaborations and alliances with external business partners.
• Represent the PVA team in internal and external meetings whilst ensuring that PVA is effectively implemented and maintained.
• Support audits and inspections related to pharmacovigilance collaborations.
• Train and educate internal teams on pharmacovigilance standards and procedures.

Required experience:

• Bachelor's degree preferably in Life Sciences.
• Minimum of 5 years of experience in the pharmaceutical industry.
• At least 3 years of specific experience in managing patient safety.
• Strong understanding of global and local pharmacovigilance regulations and guidelines.
• Proven ability to work effectively in cross-functional and international teams.

Why apply?

• Strong reputation as a specialist biopharmaceutical company.
• Opportunity to make a meaningful impact on patients with high unmet medical needs.
• Global organisation with an international pharmacovigilance and drug safety environment.
• Exposure to innovative biologics and advanced therapies.

FTE (full time equivalent) - four months (potential to extend)

Remote work - Europe based wanted

Start date: ASAP