Pharmacovigilance Associate

Pharmacovigilance Associate

Start: ASAP

End: 12 month contract (initial)

Location: Amsterdam (Hybrid, ~50% on site)

Hours: Full time (40 hrs/week)

Sector: Life Sciences | Pharmaceutical Industry | Pharmacovigilance

About the Role

A leading global healthcare organisation is looking for a Pharmacovigilance Associate to support its local pharmacovigilance activities. You will join a dynamic team responsible for ensuring patient safety and regulatory compliance across a broad portfolio of products.

In this role, you will be responsible for the accurate processing and evaluation of safety data, while contributing to compliance activities and continuous improvement of pharmacovigilance processes. You will operate in an international, matrix environment and collaborate with both internal stakeholders and external partners.

This position offers strong exposure to different therapeutic areas and the opportunity to develop within a patient-focused and highly regulated environment.

Key Responsibilities

• Manage and prioritise individual pharmacovigilance workload
• Monitor and manage PV inbox and incoming safety data
• Perform case intake, assessment, and processing activities
• Follow up with reporters (patients, healthcare professionals, vendors) to obtain additional safety information
• Ensure timely identification and escalation of potential safety, quality, or regulatory issues
• Support compliance activities in line with local and global requirements
• Maintain and update local pharmacovigilance quality documents
• Support the management of educational and risk minimisation materials
• Review safety data for trends, clusters, and potential signals
• Deliver pharmacovigilance training to internal and external stakeholders

Profile

• Bachelor's or Master's degree in Life Sciences (e.g. Pharmacy, Biomedical Sciences, Medicine or equivalent)
• Experience in the pharmaceutical industry, preferably within pharmacovigilance or a related field
• Good understanding of pharmacovigilance processes and regulatory requirements
• Strong attention to detail and ability to manage multiple priorities
• Able to work independently in a structured and compliant manner
• Effective communicator with stakeholder management skills
• Fluent in Dutch and English

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