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Pharmacovigilance Specialist
- edinburgh, scotland, G1 2AA, United Kingdom
- Permanent·Hybrid
- Full time
- £58,000 - £58,000 Per Annum
Job Description
About the Role
Our client is seeking an attentive Pharmacovigilance Specialist to join their safety surveillance team in Glasgow . This role is vital for monitoring the safety of our client's pharmaceutical products throughout their lifecycle. You will be responsible for collecting, processing, and evaluating adverse event reports, ensuring compliance with global regulatory requirements. This position offers an excellent opportunity to contribute to patient safety and pharmacovigilance best practices within a supportive team environment in Scotland .
Key Responsibilities
- Collect, assess, and document adverse event reports from various sources.
- Ensure timely and accurate reporting of safety data to regulatory authorities.
- Contribute to the preparation of periodic safety update reports (PSURs) and risk management plans.
- Liaise with internal departments and external stakeholders on safety-related matters.
- Participate in audits and inspections related to pharmacovigilance compliance.
Requirements
- Degree in Pharmacy, Nursing, Life Sciences, or a related healthcare field.
- Minimum of 2 years of experience in pharmacovigilance or drug safety.
- Thorough understanding of global pharmacovigilance regulations and guidelines (e.g., GVP).
- Experience with safety databases and adverse event reporting systems.
- Strong analytical, critical thinking, and organizational skills.
Benefits
- Competitive salary and annual performance-based pay.
- Flexible hybrid working model.
- Comprehensive health, dental, and vision insurance.
- Generous paid time off and company holidays.
- Opportunities for ongoing training and career development in pharmacovigilance.