Senior Pharmacovigilance & Safety Lead

Pfizer; Hokksund; Hybride; NOK 900 000 - 1 200 000; Plein temps

Résumé du poste

Pfizer is seeking a pharmacovigilance specialist to monitor safety programs for drugs, biologics, and medical devices. You will evaluate adverse events, support clinical trials, and ensure regulatory compliance across regions.

The role requires strong data management skills, understanding of global reporting requirements, and collaboration with cross-functional teams. Hybrid work location applies, with focus on safety evaluation and reporting activities.

Qualifications

• Experience in pharmacovigilance, data management, or clinical/research settings.
• Strong understanding of pharmaceutical development and regulatory aspects.
• Familiarity with international reporting requirements.
• Excellent organizational and time management skills to meet regulatory goals.
• Ability to solve problems and make decisions in complex situations.
• Proficiency with relational databases and data systems.
• Fluency in spoken and written English.
• Fluency in spoken and written Norwegian.

Responsabilités

• Monitor and manage the company’s drug, biologics, and medical devices surveillance program.
• Support clinical trials and post-marketing activities for compliance and safety.
• Guide operational teams in project management and resource forecasting.
• Lead or co-lead moderately complex projects and mentor team members.
• Develop and maintain expertise in products, policies, and safety databases.
• Collaborate with internal and external stakeholders on safety activities.

Connaissances

Pharmacovigilance

Regulatory compliance

Adverse event reporting

Project management

Cross-functional collaboration

Data management

English proficiency

Norwegian proficiency

Formation

BA/BS in a relevant field

MBA/MS in a related field

PhD/JD (optional seniority)

Associates degree with extensive experience

Description du poste

Pfizer is seeking a pharmacovigilance specialist to monitor safety programs for drugs, biologics, and medical devices. You will evaluate adverse events, support clinical trials, and ensure regulatory compliance across regions.

The role requires strong data management skills, understanding of global reporting requirements, and collaboration with cross-functional teams. Hybrid work location applies, with focus on safety evaluation and reporting activities.