Pharmacovigilance (PV) and Medical Information Officer - Greater Oslo Region
1 dag siden

Jobbbeskrivelse
- Location: Lysaker, Norway
- Job type: Fixed-term - 6 months contract
About The Job
As a
Pharmacovigilance (PV) and Medical Information Officer
within our North Europe MCO team, you'll play an essential role in ensuring the safety and efficacy of our pharmaceutical products while providing critical medical information support to healthcare professionals and patients. Ready to get started?
Join the team transforming how healthcare is delivered for chronic and specialty conditions worldwide. You'll help drive meaningful outcomes in diabetes, transplant, and immunology – with the scale and urgency patients deserve.
About Sanofi
We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.
Main Responsibilities
- Obtain and maintain thorough knowledge of company procedures and legal requirements regarding Pharmacovigilance and Medical Information, developing comprehensive understanding of PV and MI aspects of the company portfolio.
- Handle adverse event reports and PV data according to local legislation and company Quality Documents, providing relevant safety information to Health Authorities and stakeholders.
- Support the Country Safety Head in local safety surveillance activities, safety issues, and risk management activities.
- Manage product alerts and market research programs with timely communication to PSPV and Health Authorities.
- Handle Medical Information inquiries from Healthcare Professionals, patients, and other customers, providing high-standard services to support internal and external stakeholders.
- Collaborate effectively with applicable third parties within PV and Medical Information areas.
- Actively contribute to the North Europe Cluster PV and Medical Information team through projects and daily collaboration.
About You
- Education: University degree in Pharmacy, Medicine, or equivalent field
- Experience: Work experience in pharmaceutical industry or equivalent, preferably within pharmacovigilance or related areas
- Core competencies: Strong planning and organization skills with keen awareness of accuracy requirements; meticulous approach to work with focus on accuracy and compliance
- Communication skills: Excellent communication abilities with healthcare professionals, patients, and colleagues; strong interpersonal skills with proven track record of effective collaboration
- Team collaboration: Natural team player who thrives in collaborative environments
- Technical skills: Strong computer literacy (MS Office) and proficiency with relevant software systems
- Languages: Fluent in English and Norwegian, both written and spoken
Why choose us?
- Help shape the future of care for chronic and complex conditions like diabetes, transplant, and cardiovascular disease, making a real impact at scale with medicines that reach over 100 million people each year.
- Drive meaningful change in a streamlined, AI-powered organization that values smart, modern ways of working.
- Work in a place that combines global scale with local expertise, backed by a strong culture of collaboration and shared purpose.
- Contribute to innovations that improve outcomes, relieve pressure on healthcare systems, and expand access worldwide.
- Stretch your career in a development playground, with opportunities across functions, regions, and the entire product lifecycle.
- Join a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice.
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