Pharmacovigilance Specialist

About the Role

Our client is seeking a meticulous Pharmacovigilance Specialist to join their expanding safety team. This is a fully remote position, offering the flexibility to work from anywhere within the UK. You will play a critical role in ensuring the safety of their pharmaceutical products by monitoring, collecting, and evaluating adverse event data. Your expertise will contribute to maintaining regulatory compliance and safeguarding public health. This role is ideal for an individual who is highly organized, possesses strong analytical skills, and thrives in an independent, remote work setting, contributing vital safety insights to the company's global operations.

Key Responsibilities

• Collect, assess, and process adverse event reports from various sources.
• Ensure timely and accurate reporting of safety information to regulatory authorities.
• Conduct literature reviews for signal detection and safety assessments.
• Collaborate with internal departments and external partners on pharmacovigilance matters.
• Contribute to the development and maintenance of pharmacovigilance procedures and training materials.

Requirements

• Degree in Pharmacy, Nursing, Life Sciences, or equivalent.
• Minimum of 3 years of experience in pharmacovigilance or drug safety.
• Knowledge of global regulatory requirements for pharmacovigilance (e.g., GVP, FDA regulations).
• Strong analytical skills and attention to detail.
• Excellent written and verbal communication skills, suited for a remote-first environment.

Benefits

• Competitive salary commensurate with experience.
• Comprehensive private medical insurance.
• Generous pension contribution.
• Home office setup allowance.
• Significant opportunities for professional development and training in drug safety.