We are looking for a Senior Pharmacovigilance Officer to work within our Regulatory team. With the support of the Pharmacovigilance Manager, the main purpose of the post is to maintain oversight of safety reporting activities within the CTC, ensuring patient safety and compliance with regulatory requirements are maintained at all times.

The postholder will review SUSAR reports, raising queries with the trial teams and make timely submissions into ICSR Submissions and EudraVigilance portals, maintain oversight over SUSAR submissions and review and submit DSURs to the MHRA. A full list of duties and responsibilities can be found in the job description and person specification which can be accessed at the bottom of this page.

• This is a full-time, open-ended post, funded for 1 year in the first instance.
• Appointments will usually be made at the bottom of the salary scale.
• The CTC offers hybrid working with staff being able to work between the office and home. A minimum of 60% FTE office attendance is required for this role.
• If you have any queries about the role, please contact ctc.hr@ucl.ac.uk