Full-Time Pharmacovigilance Associate

PV Associate should be a Life science / biomedical background graduate or have other healthcare related degree qualification (chemistry, biology, biotechnology, veterinary science etc.) This is an opportunity for new graduates to start and develop their career within drug safety. The PV Associate will be working as part of a project team, performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. If you join PrimeVigilance, you can expect to work with teams of different sizes, from small clinical trial to large, generic post-marketing teams.

Responsibilities:

• Processing of Individual Case Safety Reports from all sources (post-marketing and clinical trials) in compliance with applicable regulations, PrimeVigilance procedures, and in accordance with client specific requirements and timelines, focusing on triage, data entry, quality review and submissions workflow steps.
• Reconciliation activities for all types of received reports.
• Works under supervision and mentoring of more experienced colleague.

We expect:

• Requirements: Life science / biomedical background – healthcare related degree (chemistry, biology, biotechnology, veterinary science), previous experience is not required.
• People who are excited to learn and contribute to patient safety
• Time and issue management, delegation, organization and multitasking skills with good attention to detail
• Strong interpersonal and communication skills
• Advanced English skills and Fluency in Dutch

What is the last date for applying to the job?

Which countries are accepted for this remote job?