Medicine Job at MHRA London – Advanced Clinical Research & Public Health
This medicine job at the Medicines and Healthcare products Regulatory Agency offers an outstanding opportunity for medical professionals seeking impactful jobs in London and jobs in the UK. As a Medical Assessor, you will play a vital role in assessing clinical trials, supporting regulatory decision-making, and contributing to public health through science-driven regulation.
Job Details:
- Job Position: Medical Assessor
- Location: 10 South Colonnade, Canary Wharf, London, E14 4PU, United Kingdom
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Important Dates:
- Closing Date: 7 January 2026
- Shortlisting: From 12 January 2026
- Interviews: From 2 February 2026
About the Company:
The Medicines and Healthcare products Regulatory Agency enhances and improves the health of millions of people every day through the effective regulation of medicines and medical devices, underpinned by science and research. The agency employs approximately 1300 staff working across the UK and internationally, making it a trusted employer for those seeking long-term jobs in the UK within the healthcare and regulatory sectors.
Qualifications:
- Degree in Medicine
- Registered with the General Medical Council (GMC)
- Relevant postgraduate qualification and/or experience
- Knowledge of legislation related to clinical trial regulation
Medicine Job Description:
This medicine job is based within the Clinical Investigations and Trials Function of the Innovation and Compliance Group. The Medical Assessor role involves assessing clinical aspects of clinical trial authorisation (CTA) applications and amendments, along with providing scientific and regulatory advice to companies developing new medical products. The role also supports policy and strategy development to strengthen the UK’s position as a leading destination for clinical research.
Key Responsibilities:
- Carry out risk-based assessments of data submitted in clinical trial authorisation applications
- Review chemical, biological, and advanced therapy products to protect public health
- Prepare objective assessment reports and scientific papers for advisory bodies
- Manage workload efficiently to meet regulatory deadlines
- Provide clinical trial expertise in meetings with external stakeholders
- Respond in writing to regulatory and scientific enquiries
- Build effective working relationships across internal teams and external partners
Skills & Experience Required:
- Experience in the design, conduct, and analysis of clinical trials
- Experience preparing study reports for regulatory submission or publication
- Strong decision-making and communication skills
- Ability to work in a target-driven environment
- Excellent interpersonal and teamwork abilities
Why Apply for This Medicine Job?
- Prestigious role within the Medicines and Healthcare products Regulatory Agency
- Secure government position with flexible hybrid working
- Opportunity to work on high-impact clinical research projects
- One of the most respected medicine jobs in London
- Ideal for professionals seeking meaningful jobs in the UK healthcare sector
