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LondonJob SummaryWe are currently looking for a Research Lead to join our Research and Development Function within the Scientific Research and Innovation group.This is a full-time opportunity, on a fixed term contract basis until 31st March 2028. The role will be based in 10 South Colonnade, Canary Wharf.Government departments and agencies are working towards implementing a minimum 60% attendance in office sites.Job DescriptionWho are we?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 Scientific Research and Innovation Group delivers public health impact, world-leading research innovation, and a unique regulatory proposition for patients and users via an ambitious Science Strategy which will balance innovation against sustainability and affordability. It is divided into 6 sub-Groups, Innovation Accelerator, Clinical Investigations and Trials, Research and Development, Standards Lifecycle, Control Testing and Quality Assurance and Health & Safety.The SR&I Research & Development function will deliver statutory mandated strategically aligned, sustainable and impactful Regulatory Scientific research that is applied primarily to biological reference materials development and medicines control testing and areas of international and national priority for extant and future biological medicines. Research and Development will host and nurture the current excellence in research into biologicals, biological reference materials, biological activity measurements, product quality testing and standardisation that is currently hosted by the MHRA Science Campus at South Mimms. This is a statutory activity and includes international centres of excellence such as those working on polio, influenza and the UK Stem Cell Bank.What’s the role?The postholder will join an established team and work with an SEO to match novel AMR innovations to clinical need, and identify what would be needed to enable regulatory evaluation, marketing authorisation, and access and adoption. The post holder will actively engage with national and international research partners, including academia, industry, other regulatory Agencies, and non-profit public health organisations to carry out the work and identify opportunities to leverage additional funding.The primary purpose of the role is to inform a programme of work delivering research relating to novel antimicrobials and diagnostics pertaining to AMR across One Health.An understanding of the regulatory requirements for novel and established medicines, as well as an appreciation of the opportunities and challenges of identifying and deploying AMR solutions across One Health would be desirable.The postholder will be expected to build and lead a project capable of covering the multiple disciplines and sectors that AMR encompasses, with expert knowledge of the challenges and opportunities across One Health and Lower-Middle Income Countries (LMICs). The post holder will work closely with colleagues across SR&I and other Agency groups, to provide expert advice relating to AMR products, regulation, and access.Key Responsibilities: Be accountable to the Head of Diagnostics and contribute to the strategic direction of the R&D undertaken in the team in response to programme priorities. Engage with, and provide expert advice to, national and international stakeholders including WHO, the global Pharmacopoeias, manufacturers, regulatory organisations and academia. Initiate and lead the project to pull out key regulatory and access challenges pertaining to novel AMR medicines and diagnostics. Generate scientific data that is publishable in high quality scientific journals. Establish and maintain relationships and collaborations with external stakeholders (including industry, academia, government departments, regulatory agencies and non-profit philanthropic organisations) as appropriate to identify and progress research priorities to deliver outputs that positively impact health of patients. Represent the Agency externally, nationally, and internationally, as an expert in medicinal products developed to tackle AMR and provide state of the art guidance to senior agency colleagues in other functions such as HQA and S&S. Provide expert advice on products relating to the AMR to colleagues in the Agency and other Government departments as appropriate. Seek and drive opportunities for continued service improvement through expert services, training, and scientific and technical advice.Who are we?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 Scientific Research and Innovation Group delivers public health impact, world-leading research innovation, and a unique regulatory proposition for patients and users via an ambitious Science Strategy which will balance innovation against sustainability and affordability. It is divided into 6 sub-Groups, Innovation Accelerator, Clinical Investigations and Trials, Research and Development, Standards Lifecycle, Control Testing and Quality Assurance and Health & Safety.The SR&I Research & Development function will deliver statutory mandated strategically aligned, sustainable and impactful Regulatory Scientific research that is applied primarily to biological reference materials development and medicines control testing and areas of international and national priority for extant and future biological medicines. Research and Development will host and nurture the current excellence in research into biologicals, biological reference materials, biological activity measurements, product quality testing and standardisation that is currently hosted by the MHRA Science Campus at South Mimms. This is a statutory activity and includes international centres of excellence such as those working on polio, influenza and the UK Stem Cell Bank.What’s the role?The postholder will join an established team and work with an SEO to match novel AMR innovations to clinical need, and identify what would be needed to enable regulatory evaluation, marketing authorisation, and access and adoption. The post holder will actively engage with national and international research partners, including academia, industry, other regulatory Agencies, and non-profit public health organisations to carry out the work and identify opportunities to leverage additional funding.The primary purpose of the role is to inform a programme of work delivering research relating to novel antimicrobials and diagnostics pertaining to AMR across One Health.An understanding of the regulatory requirements for novel and established medicines, as well as an appreciation of the opportunities and challenges of identifying and deploying AMR solutions across One Health would be desirable.The postholder will be expected to build and lead a project capable of covering the multiple disciplines and sectors that AMR encompasses, with expert knowledge of the challenges and opportunities across One Health and Lower-Middle Income Countries (LMICs). The post holder will work closely with colleagues across SR&I and other Agency groups, to provide expert advice relating to AMR products, regulation, and access.Key Responsibilities: Be accountable to the Head of Diagnostics and contribute to the strategic direction of the R&D undertaken in the team in response to programme priorities. Engage with, and provide expert advice to, national and international stakeholders including WHO, the global Pharmacopoeias, manufacturers, regulatory organisations and academia. Initiate and lead the project to pull out key regulatory and access challenges pertaining to novel AMR medicines and diagnostics. Generate scientific data that is publishable in high quality scientific journals. Establish and maintain relationships and collaborations with external stakeholders (including industry, academia, government departments, regulatory agencies and non-profit philanthropic organisations) as appropriate to identify and progress research priorities to deliver outputs that positively impact health of patients. Represent the Agency externally, nationally, and internationally, as an expert in medicinal products developed to tackle AMR and provide state of the art guidance to senior agency colleagues in other functions such as HQA and S&S. Provide expert advice on products relating to the AMR to colleagues in the Agency and other Government departments as appropriate. Seek and drive opportunities for continued service improvement through expert services, training, and scientific and technical advice.Person specificationMethod of assessment: A=Application, T=Test, I=Interview, P=Presentation Behaviour Criteria: Leadership (A, I) Managing a Quality Service (A, I)Experience Criteria: Significant research experience and evidence of collaborative, multidisciplinary working (A) Experience of delivering project in collaboration with external stakeholders (A, I) Evidence of engaging with external stakeholders and partners to promote knowledge exchange and build productive relationships (A, I)Technical Criteria: Demonstrate good knowledge of, and practical experience in, a broad range of research techniques used to assess and characterise biological molecules and biotherapeutics (A, I) Using AI to build data curation and collection pipelines with classification and embedding models for Natural language processing (A, I) Good knowledge of how Agency activities relate to, and support, medicines development and regulation (A, I)If you would like to find out more about this fantastic opportunity, please read our Job Description and Person Specification!Please note: The job description may not open in some internet browsers. Please use Chrome or Microsoft Edge. If you have any issue viewing the job description, please contact careers@mhra.gov.ukAlongside your salary of £60,778, Medicines and Healthcare Products Regulatory Agency contributes £17,607 towards you being a member of the Civil Service Defined Benefit Pension scheme. Find out what benefits a Civil Service Pension provides.Annual Leave: 25 days annual leave on entry, rising by one day for each completed year of service to a maximum of 30 days and pro-rata for part-time staff. PLUS 8 bank holidays Privilege Leave: 1 day Hours of Work: 37 hours (net) per week for full time staff in all geographical locations, including London and pro rata for part-time staff Occupational Sick Pay (OSP): One month full pay/one month half pay on entry, rising by one month for each completed year of service to a maximum of five months full pay/five months half pay Mobility: Mobility clause in contracts allowing staff to be mobile across the Civil ServiceCivil Service Pension Scheme. Please see the link for further information http://www.civilservicepensionscheme.org.uk/ For enquiries relating to the Civil Service Pension Schemes please contact MyCSP’s Pension Service Centre directly on 0300 123 6666 Flexible working to ensure staff maintain a healthy work-life balance Interest free season ticket loan or bike loan Employee Assistance Services and access to the Civil Service Benevolent Fund Eligibility to join Motoring , Boundless by CSMAVariety of staff and Civil Service clubs On-going learning and development Artificial intelligenceArtificial intelligence can be a useful tool to support your application, however, all examples and statements provided must be truthful, factually accurate and taken directly from your own experience. Where plagiarism has been identified (presenting the ideas and experiences of others, or generated by artificial intelligence, as your own) applications may be withdrawn and internal candidates may be subject to disciplinary action. Please see our candidate guidance (opens in a new window) for more information on appropriate and inappropriate use.Selection process detailsWe use the Civil Service Success Profiles to assess our candidates, find out more here. 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. Our applications are CV blind, and our Hiring Managers will not be able to access your CV when reviewing your application. Interview, which can include questions based on the Behaviour, Experience, Technical and Strengths Success Profiles.In the instance that we receive a high number of applications, we will hold an initial sift based on the lead criteria of Using AI to build data curation and collection pipelines with classification and embedding models for Natural language processing.Applicants are assessed on whether they meet any mandatory requirements as well as the necessary skills and experience for the role. Applications are scored based on the competency-based answers provided- ensure you have read these thoroughly and allow sufficient time. You can view the competencies for this role in the job description.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: 11th May 2026Shortlisting date: from 15th May 2026Interview date: from 27th May 2026If you need assistance applying for this role or have any other questions, please contact careers@mhra.gov.ukCandidates 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.SecuritySuccessful candidates must undergo a criminal record check.People working with government assets must complete baseline personnel security standard (opens in new window) checks.Successful candidates must undergo a criminal record check.People working with government assets must complete baseline personnel security standard (opens in new window) checks.Nationality requirementsThis Job Is Broadly Open To The Following Groups:UK nationalsnationals of the Republic of Irelandnationals of Commonwealth countries who have the right to work in the UKnationals 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 2020Turkish nationals, and certain family members of Turkish nationals, who have accrued the right to work in the Civil ServiceFurther information on nationality requirements (opens in a new window)Working for the Civil ServiceThe Civil Service Code (opens in a new window) sets out the standards of behaviour expected of civil servants.We recruit by merit on the basis of fair and open competition, as outlined in the Civil Service Commission’s recruitment principles (opens in a new window).The Civil Service embraces diversity and promotes equal opportunities. As such, we run a Disability Confident Scheme (DCS) for candidates with disabilities who meet the minimum selection criteria.The Civil Service also offers a Redeployment Interview Scheme to civil servants who are at risk of redundancy, and who meet the minimum requirements for the advertised vacancy.The Civil Service Code (opens in a new window) sets out the standards of behaviour expected of civil servants.We recruit by merit on the basis of fair and open competition, as outlined in the Civil Service Commission’s recruitment principles (opens in a new window).The Civil Service embraces diversity and promotes equal opportunities. As such, we run a Disability Confident Scheme (DCS) for candidates with disabilities who meet the minimum selection criteria.The Civil Service also offers a Redeployment Interview Scheme to civil servants who are at risk of redundancy, and who meet the minimum requirements for the advertised vacancy.Diversity and InclusionThe Civil Service is committed to attract, retain and invest in talent wherever it is found. To learn more please see the Civil Service People Plan (opens in a new window) and the Civil Service Diversity and Inclusion Strategy (opens in a new window).Once this job has closed, the job advert will no longer be available. You may want to save a copy for your records.Contact point for applicantsJob Contact :Name : The Resourcing TeamEmail : Careers@mhra.gov.ukRecruitment teamEmail : Careers@mhra.gov.ukFurther informationIn accordance with the Civil Service Commissioners’ Recruitment Principles our recruitment and selection processes are underpinned by the requirement of selection for appointment on the basis of merit by a fair and open competition. If you feel your application has not been treated in accordance with the Recruitment Principles and you wish to make a complaint, you should contact the Resourcing Team at Careers@mhra.gov.uk, in the first instance. If you are not satisfied with the response you receive you can contact the Civil Service Commission at: civilservicecommission.independent.gov.uk – info@csc.gov.uk – Civil Service Commission Room G/8 1 Horse Guards Road London SW1A 2HQ
