Pharmacovigilance Specialist Nordics

Job Overview

Biomapas is seeking a Pharmacovigilance Specialist Nordics to join their team in Denmark. This role involves ensuring drug safety and pharmacovigilance excellence across the Nordic region for global life science products, contributing significantly to public health.

Company Overview

Biomapas is a functional and full outsourcing solution provider to the global life science industry. As a trusted partner for biopharmaceutical, medical device, cosmetics, and food supplement companies, we have one-stop-shop clinical research capabilities in high recruiting countries, delivering regulatory and pharmacovigilance excellence across Europe, CIS, MENA, and LATAM regions through the entire product lifecycle. Our in-house experience combined with a hands-on mindset allows for tailored solutions to complicated challenges that emerge on your path to commercialization. Our professionals execute your projects efficiently, cost-effectively and aspire to partner with you and become an integral part of your team from Early Development to Commercial success. We keep our promises. Always.

Quick Details

• Salary Range: Market Competitive
• Job Type: Full-time
• Experience: 5 Year+
• Qualifications: Bachelor’s Degree

Key Responsibilities

• Manage and process adverse event reports in compliance with regulatory requirements.
• Ensure timely submission of safety reports to health authorities in the Nordic region.
• Conduct signal detection activities and risk-benefit assessments for assigned products.
• Contribute to the development and maintenance of pharmacovigilance systems and procedures.
• Collaborate with clients and internal teams to ensure pharmacovigilance compliance and quality.
• Provide expertise on local and international pharmacovigilance regulations.

Requirements

• Proven experience in pharmacovigilance, preferably in the Nordic region.
• Bachelor’s degree in Pharmacy, Medicine, Life Sciences, or a related field.
• Strong understanding of global and local pharmacovigilance regulations (e.g., GVP, national requirements).
• Excellent analytical skills and attention to detail.
• Proficiency in pharmacovigilance databases and safety reporting tools.
• Fluent in English; knowledge of a Nordic language is a plus.

Benefits

• Opportunity to work with a leading global life science industry service provider.
• Contribute to drug safety and public health across multiple regions.
• Professional development and growth opportunities in a dynamic environment.
• Collaborative and supportive international team culture.
• Engage in challenging and impactful projects from early development to commercial success.
• Competitive salary and benefits package.