Sanofi Hiring Pharmacovigilance (PV) & Medical Information Officer

Sanofi Hiring Pharmacovigilance (PV) & Medical Information Officer | Pharmacy/Medicine | Lysaker, Norway

Sanofi is inviting applications for the position of Pharmacovigilance (PV) and Medical Information Officer in Lysaker, Norway. This is a fixed-term, full-time opportunity (ending May 2027) within the North Europe Market Company Organization (MCO) team. The role sits at the intersection of pharmacovigilance, drug safety, regulatory compliance, and medical information services, supporting chronic and specialty therapeutic areas including diabetes, transplant, immunology, oncology, rare diseases, and vaccines.

This position is ideal for pharmacy and medical graduates with pharmaceutical industry experience who want to work in global drug safety, adverse event reporting, regulatory compliance, and medical information management within a leading R&D-driven biopharma organization.

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Company Overview

entity[“organization”,”Sanofi”,”global biopharmaceutical company”] is an R&D-driven, AI-powered global biopharmaceutical company dedicated to improving patient lives worldwide. With a strong focus on immunoscience, Sanofi develops innovative medicines and vaccines across oncology, rare diseases, neurology, cardiovascular disorders, diabetes, and immunology.

The company combines scientific expertise with digital innovation and artificial intelligence to accelerate drug discovery and lifecycle management. Sanofi’s portfolio reaches over 100 million patients annually, supported by robust pharmacovigilance systems, regulatory excellence, and global safety surveillance frameworks.

Operating across multiple regions, Sanofi emphasizes ethical compliance, patient safety, regulatory integrity, and inclusive innovation.

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Job Role & Responsibilities

The Pharmacovigilance (PV) and Medical Information Officer will ensure the safety monitoring and compliant reporting of pharmaceutical products while delivering high-quality medical information to healthcare professionals (HCPs), patients, and internal stakeholders.

Pharmacovigilance Responsibilities

• Maintain comprehensive knowledge of company pharmacovigilance procedures, legal requirements, and global safety regulations.
• Process adverse event reports in accordance with local legislation and internal quality documents.
• Provide accurate safety information to Health Authorities and relevant stakeholders.
• Support the Country Safety Head in safety surveillance, risk management, and signal management activities.
• Manage product alerts and market research program communications with Pharmacovigilance and Health Authorities.
• Ensure compliance with global safety reporting timelines and regulatory obligations.

Medical Information Responsibilities

• Respond to medical information inquiries from healthcare professionals, patients, and other stakeholders.
• Provide scientifically accurate, compliant, and balanced responses aligned with approved labeling and company standards.
• Maintain documentation of medical information activities in compliance with quality and regulatory requirements.
• Collaborate with internal departments including regulatory affairs, medical affairs, and quality teams.

Cross-Functional Collaboration

• Work closely with third-party partners involved in PV and Medical Information activities.
• Contribute actively to North Europe Cluster projects and operational initiatives.
• Ensure accurate documentation and adherence to pharmacovigilance quality systems.

This role demands precision, regulatory awareness, strong communication skills, and the ability to operate within structured pharmacovigilance and compliance frameworks.

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Eligibility & Qualifications

Educational Qualification

University degree in:
Pharmacy, Medicine, Clinical Pharmacology, Biomedical Sciences, Life Sciences, or equivalent medical/healthcare discipline.

Experience

• Prior experience in the pharmaceutical industry or equivalent healthcare setting.
• Experience in pharmacovigilance, drug safety, medical information, or regulatory compliance preferred.

Core Competencies

• Strong planning and organizational skills.
• High level of accuracy and attention to detail.
• Compliance-driven mindset with understanding of regulatory obligations.
• Ability to manage safety data and medical information requests efficiently.

Communication & Language Skills

• Excellent written and verbal communication skills.
• Ability to interact professionally with healthcare professionals and patients.
• Fluency in English and Norwegian (both written and spoken) is mandatory.

Technical Skills

• Strong computer literacy including Microsoft Office tools.
• Experience working with pharmacovigilance databases and medical information systems preferred.

Candidates must demonstrate regulatory awareness, structured documentation capability, and strong collaboration skills.

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Location & Employment Details

• Location: Lysaker, Norway
• Employment Type: Full-Time
• Contract Type: Fixed-Term (ending May 2027)
• Department: Pharmacovigilance & Medical Information

Application Process

Interested candidates can apply directly through Sanofi’s official careers portal using the link below:

Apply Here: https://jobs.sanofi.com/en/job/-/-/2649/34335990720

Applicants should highlight their pharmacovigilance experience, adverse event handling exposure, regulatory compliance knowledge, and medical information expertise in their application.

Career Growth Opportunities

With experience, professionals can advance into roles such as:

• Senior Pharmacovigilance Officer
• Drug Safety Manager
• Risk Management Specialist
• Medical Information Manager
• Regulatory Affairs & Safety Lead

The increasing global emphasis on drug safety, benefit-risk evaluation, and regulatory intelligence ensures strong long-term career stability in pharmacovigilance and medical affairs.

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Frequently Asked Questions (FAQs)

1. Is prior pharmacovigilance experience required?

Experience in pharmacovigilance or related pharmaceutical roles is preferred but not strictly limited to PV-only backgrounds.

2. Is Norwegian language proficiency mandatory?

Yes, fluency in both English and Norwegian is required.

3. Is this a permanent role?

No, this is a fixed-term contract ending May 2027.

4. What therapeutic areas are involved?

The role supports chronic and specialty areas including diabetes, transplant, immunology, oncology, rare diseases, and vaccines.

5. Does the role involve regulatory reporting?

Yes, the position includes handling adverse event reports and supporting regulatory compliance activities.

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Summary Table

Company	Sanofi
Vacancies	Pharmacovigilance (PV) & Medical Information Officer
Required Education	Pharmacy, Medicine, Biomedical Sciences, Clinical Pharmacology
Experience	Pharmaceutical industry experience; PV or medical information exposure preferred