Senior Pharmacovigilance Agreements Manager(m/w/x)

Description

You will lead the strategic lifecycle of pharmacovigilance agreements, ensuring global compliance and patient safety through expert negotiations and seamless cross-functional collaboration.

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

Benefits