Pharmacovigilance Specialist

About the Role

Our client is seeking a detail-oriented Pharmacovigilance Specialist to join their dedicated safety team in Manchester . In this critical role, you will be responsible for the collection, assessment, and reporting of adverse events associated with their pharmaceutical products. Your vigilance will ensure patient safety and regulatory compliance, contributing to the responsible management of their product portfolio. This office-based position offers the opportunity to work within a highly collaborative environment, focused on maintaining the highest standards of drug safety.

Key Responsibilities

• Collect, review, and assess adverse event reports from various sources.
• Ensure timely and accurate reporting of safety information to regulatory authorities and internal stakeholders.
• Contribute to the preparation of Periodic Safety Update Reports (PSURs) and Risk Management Plans (RMPs).
• Participate in signal detection activities and risk assessment processes.
• Liaise with external partners and internal departments on pharmacovigilance matters.
• Maintain the pharmacovigilance database and ensure data quality.

Requirements

• Degree in Medicine, Pharmacy, Nursing, or Life Sciences.
• At least 3 years of experience in pharmacovigilance within the pharmaceutical industry.
• Strong knowledge of global pharmacovigilance regulations and reporting requirements.
• Experience with pharmacovigilance databases and safety reporting systems.
• Excellent analytical and problem-solving skills.
• High level of accuracy and attention to detail.

Benefits

• Attractive annual salary with potential for annual increases.
• Comprehensive health, dental, and optical coverage.
• Generous pension contribution.
• On-site amenities and a supportive work environment.
• Opportunities for professional growth and development within the company.