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Senior Pharmacovigilance Agreements Manager(m/w/x)
Managing end-to-end Pharmacovigilance Agreements for rare disease therapies. 3+ years managing patient safety alliances or partnerships required. Global cross-functional collaboration.
Anforderungen
- 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
Aufgaben
- 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
Berufserfahrung
- 5 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Attraktive Vergütung
- Competitive compensation
Familienfreundlichkeit
- Emphasis on work/life balance
Karriere- und Weiterentwicklung
- Professional growth opportunities
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Senior Pharmacovigilance Agreements Manager(m/w/x)
Managing end-to-end Pharmacovigilance Agreements for rare disease therapies. 3+ years managing patient safety alliances or partnerships required. Global cross-functional collaboration.
Anforderungen
- 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
Aufgaben
- 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
Berufserfahrung
- 5 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Attraktive Vergütung
- Competitive compensation
Familienfreundlichkeit
- Emphasis on work/life balance
Karriere- und Weiterentwicklung
- Professional growth opportunities
Über das Unternehmen
Sobi
Branche
Pharmaceuticals
Beschreibung
The company is a specialized biopharmaceutical company dedicated to rare diseases and committed to developing innovative therapies.
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