Pharmacovigilance Specialist

About the Role

Our client is seeking a dedicated Pharmacovigilance Specialist to join their safety surveillance team in Brighton . This role is crucial for monitoring the safety of pharmaceutical products once they are on the market, ensuring that potential risks are identified, assessed, and managed effectively. You will be responsible for collecting, processing, and reporting adverse event data, contributing to the overall safety profile of our client's medicines. This is an excellent opportunity to work in a vital area of pharmaceutical science, contributing to patient safety and regulatory compliance from their offices in Brighton , with a flexible hybrid working model.

Key Responsibilities

• Collect, process, and document adverse event reports from various sources.
• Ensure timely and accurate reporting of safety information to regulatory authorities and internal stakeholders.
• Maintain and update the pharmacovigilance database.
• Participate in signal detection activities and contribute to risk management plans.
• Collaborate with medical, regulatory, and clinical teams on safety-related matters.

Requirements

• Bachelor's degree in a life science, nursing, or pharmacy-related field.
• 1-3 years of experience in pharmacovigilance or drug safety.
• Familiarity with adverse event reporting processes and regulatory requirements (e.g., GVP).
• Strong attention to detail and excellent data entry skills.
• Good understanding of medical terminology and ability to work collaboratively.

Benefits

• Competitive salary and annual bonus opportunities.
• Comprehensive private medical insurance and wellness programs.
• Generous pension contribution and paid time off.
• Support for professional development and training in pharmacovigilance.
• Hybrid work arrangement offering a balance between office collaboration in Brighton and remote flexibility.