Senior Pharmacovigilance Agreements Manager(m/w/x)

Requirements

• Bachelor's degree in Life Sciences or relevant scientific discipline
• Minimum 5 years pharmaceutical industry experience in pharmacovigilance, regulatory affairs, or quality assurance
• At least 3 years experience managing patient safety alliances or partnership
• Understanding of global and local pharmacovigilance regulations and guidelines
• Excellent negotiation, communication, and problem-solving skills
• Ability to work in cross-functional and international teams
• Strong organizational skills and project management ability
• Leadership skills for meetings, negotiations, and training
• Proficiency in written and spoken English
• Behaviors aligned with Care, Ambition, Urgency, Ownership, and Partnership

Tasks

• Manage the end-to-end lifecycle of Pharmacovigilance Agreements
• Develop and execute PVA maintenance and termination
• Contribute to strategic planning with line management
• Advise global functions on commercial and access programs
• Embed compliant pharmacovigilance obligations into agreements
• Align internal patient safety and cross-functional departments
• Oversee collaborations with external business and healthcare partners
• Negotiate roles and responsibilities within pharmacovigilance agreements
• Partner with Global Pharmacovigilance to implement PVAs
• Provide expertise on evolving pharmacovigilance regulations
• Implement communication and risk management collaboration strategies
• Represent the PVA function in stakeholder meetings
• Support pharmacovigilance audits and inspection CAPA plans
• Train internal teams on pharmacovigilance standards
• Identify process improvements and risk mitigation opportunities
• Deputize for the Global PV Licensing Director

Work Experience

Education

Languages