Full-Time Senior Pharmacovigilance Associate

Senior PV Associate should have a Life science/bio medical background graduate or other healthcare-related degree (chemistry, biology, biotechnology, veterinary science, etc.).

Opportunity for new graduates to start and develop their career in drug safety.

Working as part of a project team, performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance.

Expect to work with teams of different sizes, from small clinical trials to large, generic post-marketing teams.

Responsibilities include:

• Processing of Individual Case Safety Reports (post-marketing and clinical trials) complying with regulations, PrimeVigilance procedures, and client requirements & timelines.
• Focusing on triage, data entry, quality review, and submissions workflow.
• Reconciliation activities for all types of reports.

Works under supervision and mentoring of more experienced colleagues.

Requirements include:

• Life science/bio medical background – healthcare-related degree (chemistry, biology, biotechnology, veterinary science). No previous experience required.
• Excited to learn and contribute to patient safety.
• Time and issue management, delegation, organization, multitasking, and attention to detail.
• Strong interpersonal and communication skills.
• Advanced English skills (verbal and written), at least B2 level.

Additional notes:

• Diversity, equity, and inclusion are prioritized.
• Training and career development opportunities are provided.
• Emphasis on personal and professional growth.
• Friendly and supportive work environment.
• Opportunity to work with colleagues worldwide.
• Company language: English.
• Core values: Quality, Integrity, Trust, Drive, Passion, Agility, Responsiveness, Belonging, Collaborative Partnerships

What is the last date for applying to the job?

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