Pharmacovigilance Specialist

About the Role

Our client is seeking a dedicated Pharmacovigilance Specialist to contribute to their safety monitoring and reporting team in Derby . This role is critical for ensuring patient safety by monitoring, detecting, and reporting adverse events associated with pharmaceutical products. You will be responsible for case processing, data analysis, and ensuring compliance with global regulatory requirements for pharmacovigilance. The position offers an excellent opportunity for individuals passionate about drug safety and regulatory compliance, working within a supportive team environment in Derby .

Key Responsibilities

• Process and evaluate adverse event reports from various sources, ensuring timely and accurate data entry.
• Perform safety data analysis and identify potential safety signals for further investigation.
• Prepare and submit regulatory safety reports (e.g., DSURs, PADERs) to health authorities.
• Ensure compliance with global pharmacovigilance regulations and guidelines.
• Contribute to the development and maintenance of pharmacovigilance procedures and training materials.
• Liaise with internal departments and external partners on safety-related matters.

Requirements

• Bachelor's degree in Pharmacy, Nursing, Life Sciences, or a related healthcare field.
• Minimum of 2 years of experience in pharmacovigilance or drug safety.
• Solid understanding of global pharmacovigilance regulations and reporting requirements.
• Experience with safety database systems and adverse event case processing.
• Strong attention to detail, organizational skills, and ability to manage multiple tasks.
• Good written and verbal communication skills.

Benefits

• Competitive salary and comprehensive benefits package.
• Opportunities for professional development and training in pharmacovigilance.
• Pension scheme and life assurance.
• Generous annual leave allowance.
• Flexible working arrangements with hybrid model, based in Derby .
• Supportive team culture focused on patient safety.