Full Time • Contract

Pharmacovigilance & Medical Information Officer

Sanofi
Lysaker, Norway
Competitive Salary
Posted 19/02/2026

About the Role

Roles & Responsibilities
• Handle adverse event case processing in compliance with local regulations and company quality standards
• Maintain updated knowledge of pharmacovigilance and medical information procedures
• Support the Country Safety Head in local safety surveillance and risk management activities
• Manage product alerts, safety communications, and market research safety programs
• Respond to medical information inquiries from healthcare professionals, patients, and stakeholders
• Ensure timely reporting to Health Authorities and internal safety teams
• Collaborate with third-party vendors and internal PV/MI stakeholders
• Contribute to North Europe Cluster PV and Medical Information projects
• Ensure compliance with regulatory requirements and internal SOPs

Qualification
• Bachelor's or Master's degree in Pharmacy
• Degree in Pharmacy, Medicine, Life Sciences, or equivalent discipline

Experience
• Experience in the pharmaceutical industry
• Prior experience in Pharmacovigilance, Drug Safety, or Medical Information preferred

Skills
• Strong attention to detail and regulatory compliance
• Excellent planning and organizational abilities
• Ability to work effectively in a cross-functional, global team
• Proficiency in MS Office and safety databases
• Fluency in English and Norwegian (written and spoken)

About the Company
Sanofi is a global R&D-driven biopharmaceutical leader focused on innovative therapies in areas such as diabetes, immunology, transplant, and specialty care, committed to advancing patient safety and improving health outcomes worldwide.

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Pharmacovigilance & Medical Information Officer at Sanofi | Jobslly