Description

We are currently looking for an Associate Scientific Assessor to join our Benefit Risk Evaluation I Function within the Safety & Surveillance group.

Location & Working Conditions

The role will be based in 10 South Colonnade Canary Wharf London E14 4PU and is available only within the UK. It is a full‑time opportunity on a 12 month fixed‑term contract or temporary promotion basis. We are implementing a flexible hybrid way of working with a minimum of 8 days per month on site, which may flex up to 12 days depending on business needs.

Who We Are

The Medicines and Healthcare products Regulatory Agency enhance and improve the health of millions of people every day through the effective regulation of medicines and medical devices underpinned by science and research. The Safety and Surveillance Group brings together a single integrated structure of devices and medicines safety expertise with enforcement capabilities.

Safety & Surveillance Group Purpose

• Ensure a world class comprehensive vigilance system that can promptly detect and monitor signals across the product life cycle.
• Evaluate the benefit risk of medicines and devices for which signals or other safety concerns emerge and develop effective and measurable risk mitigation measures.
• Ensure patients and other stakeholders are involved in the regulatory processes and appropriate messages are issued for patients and stakeholders following regulatory decisions.
• Deploy innovative interventions to reduce the criminal threat.
• Exploiting data and embracing new technologies to develop the evidence to support our actions and understand their impact.

Therapeutic Areas Covered

• Oncology, Haematology, Thrombotic disease
• Musculoskeletal, Trauma and Cosmetic
• Biosafety, Nonclinical and Emerging Technologies
• Respiratory, Imaging and Critical Care
• Vaccines, Infectious Diseases and Diagnostics
• Cardiovascular and Fluid Management
• Skin, Senses, Movement and Pain
• Metabolic, and Renal Systems
• Psychiatric Disorders, Cognition and Mental Health
• Gastrointestinal System, Nutrition, Endocrine and Fertility

Key Responsibilities

• Ensuring the quality and accuracy of Sentinel records.
• Assist BRE assessment teams with the processing of variation applications related to safety and applications to renew market authorisations.

Candidate Profile

• A degree in pharmacy, pharmacology, nursing, physiology, toxicology or another relevant life science discipline.
• Excellent IT skills and attention to detail, combined with a desire to ensure that accurate product information is made publicly available.
• Experience working in a regulatory environment or other relevant area and familiarity with associated systems.
• Ability to analyse and interpret data and make appropriate recommendations under pressure.
• Confidence and ability to work as part of a team in a fast‑paced environment.
• Excellent written and verbal communication skills.

Application Process

The selection process includes the Civil Service Success Profiles, an online application form, and an interview. Applicants will be assessed against mandatory requirements and necessary skills and experience. Questions focus on Behaviour, Experience, Technical, and Strengths Success Profiles.

Closing Dates

Closing date: 16 September 2025

Shortlisting date: From 17 September 2025

Interview date: Week commencing 22 September 2025