Pharmacovigilance Specialist, Case Processing

Overview

In this Pharmacovigilance role, you will manage daily adverse event case processing, including MedDRA coding, seriousness assessments, and follow-up activities to ensure high-quality safety data. You will prepare narratives, deliver client notifications, and contribute to training materials while staying current with global safety regulations. You will work within a cross-functional PV team to de-risk and accelerate client programs across regulated medicines and devices. This hybrid, globally aware role offers opportunities to influence safety outcomes and build expertise in a trusted advisory environment.

Pay / Benefits

• remote work options
• hybrid work arrangement
• inclusive workplace
• training and development opportunities

Responsibilities

• Daily adverse event case processing (clinical trial and post-marketed)
• MedDRA coding and determining seriousness and expectedness
• Follow-up information gathering
• Create and review case narratives
• Client notifications for case management
• Support development and delivery of training materials
• Highlight discrepancies to PV leadership
• Maintain up-to-date knowledge of global safety regulations
• Peer reviews for quality and consistency
• Other duties as assigned

Key requirements

• Bachelor in Life Sciences
• Two years of related work experience
• Strong verbal and written communication
• High attention to detail and accuracy
• Ability to work independently and in a multidisciplinary team
• Basic knowledge of pharmacovigilance
• Ability to identify and resolve problems in a timely manner

• communication
• attention to detail
• problem solving
• MedDRA coding
• Pharmacovigilance basics
• Knowledge of global safety regulations

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