Monitor product safety remotely using adverse event analysis and signal detection for a globally recognized biopharmaceutical company. Work autonomously while communicating proactively.

This senior pharmacovigilance role supports continuous safety monitoring and regulatory reporting. You will assess adverse events, prepare safety documents, and contribute to risk management strategies. Collaboration spans clinical operations, medical affairs, regulatory affairs, authorities, and external partners globally.

Key Responsibilities:

- Oversee adverse event collection, processing, and reporting
- Conduct medical and scientific causality assessments
- Detect safety signals and support risk management strategies
- Prepare PSURs, PBRERs, and regulatory safety documents




- Ensure FDA, EMA, ICH, and SOP compliance

Requirements:

- Degree in pharmacy, medicine, nursing, or life sciences
- Minimum six years pharmacovigilance or drug safety experience
- Knowledge of global regulations and reporting requirements
- Experience with case processing, medical assessment, and signal detection
- Proficiency in safety databases and office software

Apply senior pharmacovigilance expertise, analytical judgment, and regulatory knowledge to protect patients through global safety surveillance.

📌 Remote Senior Pharmacovigilance Officer (Kimberley)
🏢 Placements24
📍 Kimberley