Pharmacovigilance Specialist

About the role

ProPharma is seeking a Pharmacovigilance Specialist to join its safety team. You will be responsible for processing adverse event cases from clinical trials and post‑marketing sources, ensuring compliance with global safety regulations.

Key responsibilities

• Daily processing of adverse event cases, including MedDRA coding, seriousness and expectedness assessment.
• Conduct case follow‑up activities and gather required information.
• Create and review case narratives and provide client notifications as needed.
• Support development and delivery of training materials.
• Highlight discrepancies to senior PV staff and perform peer reviews for quality and consistency.
• Maintain up‑to‑date knowledge of global safety regulations.

Required profile

• Bachelor’s degree in life sciences (advanced degree, RN, RPh, PharmD preferred).
• Minimum two years of relevant experience in pharmacovigilance or drug safety.
• Strong verbal, written and interpersonal communication skills.
• High level of accuracy, attention to detail, and ability to work independently and within a multidisciplinary team.

Required skills

• MedDRA coding.
• Basic knowledge of pharmacovigilance processes.

What we offer

• Inclusive, diverse workplace that values authenticity.
• Opportunities for remote and hybrid work arrangements.
• Professional development and training support.