Non-Clinical Assessor (Biological) - £60,778 – £68,422 p.a. + benefits

We are currently looking for a Non-Clinical Assessor (Biological) to join our Innovative Medicines Function within the Healthcare and Quality Access group.

This is a full-time opportunity, on a permanent basis. The role will be based in 10 South Colonnade, Canary Wharf London, E14 4PU.

The objective of the Healthcare Quality and Access portfolio is to drive quality and critically appraise benefits and risks to inform robust decisions on healthcare access including accelerated access pathways. It will do this by bringing together a fusion of our capabilities across both medicines and medical devices to enable licensing and market access, as well as ensuring compliance with regulations and standards.

The Innovative Medicines function delivers a risk appropriate critical appraisal of quality, safety and efficacy of innovative medicinal products, determining whether a product’s benefits outweighs the risks. It aims to accelerate their route to market to drive earlier patient access. Through this function the Agency will be seen as a leader in facilitating early access to safe and innovative medicines attracting the life sciences sector and contributing to a positive patient experience and to the improvement of public health outcomes.

Reporting to the Head of Biologicals team, a Non-clinical Assessor (Biologicals) evaluates the pre-clinical and environmental risk aspects of marketing authorisation, Early Access to Medicines (EAMs), Innovative Licensing and Access Pathway (ILAP) and clinical trial applications for medicinal products and make decisions on their suitability for approval.

This role encompasses the evaluation of a range of new biological medicinal products, including new active substances, advanced therapies, and other innovative products at different stages of development, as well as their environmental impact. The role also contributes to the development of regulatory policy, scientific guidance, and legislative frameworks relating to innovative medicinal products and emerging technologies. The reports written and recommendations made will be highly influential in initiating trials of new medicines and taking these through clinical development, and/or allowing new medicines to be made widely available to patients.

The post offers career development and progression opportunities in line with our internal development programme (scheme structure currently under review).

Key responsibilities

Service delivery

• Carry out the assessment of pre-clinical data provided in marketing authorisation and clinical trial authorisation applications for biological products, making appropriate recommendations and decisions in line with the protection of public health.
• Involvement in the ILAP and EAMs scheme, and provision of scientific advice on the non-clinical aspects and/or environmental aspects of drug development.
• Contribute to the drafting, review, implementation, and other cross-functional activities associated with development of legislation, scientific guidance, and policy documents relating to medicinal products and emerging technologies.
• Manage own workload, working in conjunction with other assessors to meet agency deadlines.
• Prepare and present objective assessments or other scientific papers to expert advisory bodies.

Service improvement

• Contribute to development of assessment policy, regulatory guidance, legislative implementation, and scientific practice; and proactively identify where such contributions would be beneficial.
• Contribute to divisional procedures and proactively identify where such contributions would be beneficial.

Quality and Assurance

• Promptly update agency, divisional or team work management databases to reflect the progress of own’s work.
• Display a high level of attention to detail to ensure up to date, accurate data and documents are held on internal databases.
• Use own and agency resources in line with agency and divisional strategy to meet targets
• Support the generation and evaluation of evidence from internal and external sources to inform decision making, policy development, and continuous improvement.

Leadership and management

• Lead or contribute to multidisciplinary projects involving internal and external stakeholders to support regulatory, scientific and policy objectives.
• Develop to provide ad hoc advice to colleagues in the Division or Agency.
• Extend and deepen skills and knowledge in relevant scientific or professional areas.

General

• Develop good working relationships and communicate effectively with colleagues and other internal and external stakeholders, including government departments, healthcare organisations, academia, industry and patient representatives.
• Participate in other ad-hoc tasks/projects as requested by the Unit Manager.

The job description is not intended to be exhaustive and it is likely that responsibilities and outcomes may be altered from time to time in the light of changing circumstances and after consultation with the postholder.

Degree in molecular biology, toxicology, pharmacology, immunology or other appropriate life science .

This job is broadly open to the following groups:

• UK nationals
• nationals of the Republic of Ireland
• nationals of Commonwealth countries who have the right to work in the UK
• nationals of the EU, Switzerland, Norway, Iceland or Liechtenstein and family members of those nationalities with settled or pre-settled status under the European Union Settlement Scheme (EUSS) (opens in a new window)
• nationals of the EU, Switzerland, Norway, Iceland or Liechtenstein and family members of those nationalities who have made a valid application for settled or pre-settled status under the European Union Settlement Scheme (EUSS)
• individuals with limited leave to remain or indefinite leave to remain who were eligible to apply for EUSS on or before 31 December 2020
• Turkish nationals, and certain family members of Turkish nationals, who have accrued the right to work in the Civil Service

Further information on nationality requirements (opens in a new window)

This vacancy is using Success Profiles (opens in a new window), and will assess your Behaviours, Strengths, Experience and Technical skills.

• Online application form, including questions based on the Behaviour, Experience and Technical Success Profiles. Please ensure all application questions are completed in full; your application may not be considered if any responses are left blank.
• Presentation, to be prepared as part of your interview, with further information being supplied when you reach this stage.
• Interview, which can include questions based on the Behaviour, Experience, Technical and Strengths Success Profiles.
• An anonymised CV outlining your job history and previous skills/experience that demonstrate how you meet the essential criteria.

In the instance that we receive a high number of applications, we will hold an initial sift based on the lead criteria of: Up to date specialist level of knowledge in one or more relevant scientific areas or broader knowledge across the range of scientific activities in relation to the non-clinical development of human medicinal products, including biological products, and advanced therapies.

If you require any disability related adjustments at any point during the process, please contact careers@mhra.gov.uk as soon as possible.

Closing date: 25 September 2026

Shortlisting date: From 26 September 2026

Interview date: From 05 October 2026

If you need assistance applying for this role or have any other questions, please contact careers@mhra.gov.uk

Candidates will be subject to UK immigration requirements as well as Civil Service nationality rules. Further information on whether you are able to apply is available here.

Successful candidates must pass a disclosure and barring security check as well as animal rights and pro-life activism checks. People working with government assets must complete basic personnel security standard checks.

Certain roles within the MHRA will require post holders to have vaccinations, and in some circumstances, routine health surveillance. These roles include:

• Laboratory-based roles working directly with known pathogens
• Maintenance roles, particularly those required to work in laboratory settings
• Roles that involve visiting other establishments where vaccination is required
• Roles required to travel overseas where specific vaccination may be required.

Applicants who are successful at interview will be, as part of pre-employment screening subject to a check on the Internal Fraud Database (IFD). This check will provide information about employees who have been dismissed for fraud or dishonesty offences. This check also applies to employees who resign or otherwise leave before being dismissed for fraud or dishonesty had their employment continued. Any applicant’s details held on the IFD will be refused employment. A candidate is not eligible to apply for a role within the Civil Service if the application is made within a 5 year period following a dismissal for carrying out internal fraud against government.

Any move to the MHRA from another employer will mean you can no longer access childcare vouchers. This includes moves between government departments. You may however be eligible for other government schemes, including Tax-Free Childcare. Determine your eligibility here.

Individuals appointed on level transfer will retain their existing salary and are responsible for ensuring they fully understand the financial implications of any potential move and the impact (if any) on their terms. If an individual is in any doubt, they should seek clarification before accepting a job offer.

Staff joining on promotion will receive up to a 10% increase of their current basic salary, or the pay band minimum, whichever is the greater.

The individual will not retain any allowances paid by the former department/Agency, unless there are special circumstances, such as a reserved right to those allowances on transfer.

Successful candidates may be subject to annual Occupational Health reviews dependent on role requirements. If you have any queries, please contact careers@mhra.gov.uk.

Feedback will only be provided if you attend an interview or assessment.