Safety Information Manager
2 days ago
This is a full-time opportunity to join our Centre for Drug Development (CDD) on a maternity cover contract for 14 months.
The successful candidate will lead a small Pharmacovigilance (PV) team responsible for the processing and reporting of safety information on our clinical trials.
The ideal candidate will have significant experience in pharmacovigilance, working with safety databases, and electronic regulatory submissions.
Key Responsibilities:- Oversee procedures for collection, processing, and reporting of serious adverse events, urgent safety measures, and other safety information from clinical trials sponsored by Cancer Research UK.
- System owner of the electronic safety database, working with the Technology department to ensure its proper selection, validation, maintenance, and use in accordance with SOPs and regulatory guidelines.
- Monitor and ensure compliance of regulatory reporting of safety information.
- Respond to audit and inspection findings, identifying and implementing corrective and preventive actions as appropriate.
We estimate the salary for this role to be around £65,000 - £85,000 per annum, depending on location and experience.
About Us:Cancer Research UK is a world-leading charity dedicated to saving lives through research into cancer. We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities, and high-quality tools.
Our policies and processes enable you to improve your work-life balance, take positive steps in your career, and achieve your personal wellbeing goals.
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