Pharmacovigilance Specialist

About the Role

Our client, a key player in the pharmaceutical industry , is actively seeking a dedicated Pharmacovigilance Specialist to join their team in Durban . This role is crucial for ensuring the safety of pharmaceutical products by monitoring, detecting, and reporting adverse events. You will play a vital role in maintaining regulatory compliance and contributing to the overall safety profile of our client's medicines.

This is an excellent opportunity for individuals passionate about patient safety and regulatory affairs within the dynamic pharmaceutical landscape.

• Receive, process, and evaluate adverse event reports from various sources (healthcare professionals, consumers, clinical trials).
• Ensure timely and accurate reporting of safety information to regulatory authorities worldwide according to global regulations.
• Conduct literature reviews for potential safety signals and contribute to signal detection activities.
• Participate in the development and updating of safety-related documents, such as Investigator Brochures and Risk Management Plans.
• Collaborate with internal departments (e.g., Regulatory Affairs, Medical Affairs, Clinical Development) on safety matters.

• Degree in Pharmacy, Nursing, Life Sciences, or a related field.
• Minimum of 3 years of experience in pharmacovigilance or drug safety within the pharmaceutical sector.
• Thorough understanding of global drug safety regulations and reporting requirements (e.g., CIOMS, FDA, EMA).
• Experience with pharmacovigilance databases and safety reporting systems.
• Strong analytical skills and attention to detail for accurate data assessment and reporting.

• Competitive salary commensurate with experience.
• Flexible remote work arrangements available.
• Comprehensive health and wellness benefits.
• Opportunities for professional growth and specialized training in drug safety.
• A commitment to fostering a culture of safety and continuous improvement.