Roche
Group Director, PV Intelligent Automation and Business Systems Solutions (PVIS)(m/w/x)
Full-timeWith HomeofficeSenior
Basel
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SOSobi
Senior Pharmacovigilance Agreements Manager(m/w/x)
Basel
Full-timeWith Home OfficeSenior
Nejo AI Summary
Managing end-to-end Pharmacovigilance Agreements for rare disease therapies. 3+ years managing patient safety alliances or partnerships required. Global 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
Work Experience
- 5 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Competitive Pay
- Competitive compensation
Family Support
- Emphasis on work/life balance
Career Advancement
- Professional growth opportunities
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Sobi and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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SOSobi
Senior Pharmacovigilance Agreements Manager(m/w/x)
Basel
Full-timeWith Home OfficeSenior
Nejo AI Summary
Managing end-to-end Pharmacovigilance Agreements for rare disease therapies. 3+ years managing patient safety alliances or partnerships required. Global 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
Work Experience
- 5 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Competitive Pay
- Competitive compensation
Family Support
- Emphasis on work/life balance
Career Advancement
- Professional growth opportunities
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Sobi and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
Sobi
Industry
Pharmaceuticals
Description
The company is a specialized biopharmaceutical company dedicated to rare diseases and committed to developing innovative therapies.
Not a perfect match?
- Roche
Group Director, PV Intelligent Automation and Business Systems Solutions (PVIS)(m/w/x)
Full-timeWith HomeofficeSeniorBasel - Novartis
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Full-timeWith HomeofficeSeniorBasel - Novartis Pharma AG
Head Legal Medical Affairs, International(m/w/x)
Full-timeWith HomeofficeSeniorBasel - Novartis Pharma AG
Director - Pipeline Governance(m/w/x)
Full-timeWith HomeofficeSeniorBasel - Revolution Medicines
Senior Director, Compliance(m/w/x)
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