Platform Delivery Lead at Medicines and Healthcare Regulatory Agency

London, England, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

27 Apr, 26

Salary

0.0

Posted On

27 Jan, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Communication Skills, Organizational Skills, Problem Solving, Data Analysis, Project Management, Stakeholder Engagement, Teamwork, Customer Service, Technical Communication, Leadership, Automation, Reporting, Risk Management, Clinical Trials, Regulatory Compliance, IT Skills, Science Discipline

Industry

Government Administration

Description

We are currently looking for a Platform Delivery Lead to join our Clinical Investigations and Trials Function within the Innovation and Compliance group. This is a full-time opportunity, on a fixed term contract basis until 31st March 2027. The role will be based in 10 South Colonnade, Canary Wharf London, E14 4PU. Government departments and agencies are working towards implementing a minimum 60% attendance in office sites. We are currently implementing a flexible, hybrid way of working, with a minimum of 8 days per month working on site to enable the collaboration and contact with partners and stakeholders needed to deliver MHRA business. Attendance on site is driven by business needs so depending on the nature of the role, this can flex up to 12 days a month, with the remainder of time worked either remotely or in the office. Some roles will need to be on site more regularly. Remote working is potentially available for some specific roles. Please discuss this with the recruiting manager before accepting an appointment. 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 Innovation and Compliance Group delivers public health impact, world-leading research innovation, and a unique proposition via an ambitious Science Strategy which will balance innovation against sustainability and affordability. It is divided into four sub-Groups: Innovation Accelerator and Regulatory Science, Clinical Investigations and Trials, Standards and Compliance and Innovative Devices. The Clinical Investigations and Trials function provides efficient, pragmatic, proportionate and patient-centred advice for, and assessment of, clinical investigations into the performance and safety of medical devices and diagnostics as well as clinical trials of investigational medicinal products. What’s the role? This key role will be critical in maintaining and enhancing the reputation of the UK as a great place to conduct clinical research for medicines and devices. The role holder will be responsible for driving work in collaboration with the HRA to develop an IT platform for a modernised end-to-end service of clinical trial applications. This is an opportunity to modernise processes, improve data use, increase automation, improve reporting and support risk-proportionate decision-making in clinical trial assessments within MHRA and supporting the NHS 10-year plan and the Life Sciences Sector Plan (LSSP). Key responsibilities: Driving the collaborative development and implementation of a modernised, end-to-end clinical trial application service in partnership with the Health Research Authority (HRA) and other MHRA teams, ensuring alignment with the replacement of the Integrated Research Application System (IRAS) under the Research Systems Programme (RSP). Leading the modernisation of clinical trial processes, focusing on enhancing data utilisation, increasing automation, and improving reporting capabilities to support risk-proportionate decision-making in line with the Medicines and Healthcare products Regulatory Agency (MHRA) and NHS 10-year Health Plan objectives. Leading the transition from the current IRAS and Appian systems, addressing integration challenges and minimising disruption to ongoing services through effective project planning and stakeholder engagement. Provide regular progress updates and analysis to senior management, highlighting risks, opportunities, and the impact of system changes on clinical trial assessment efficiency and quality. Who are we looking for? Our successful candidate will have: Excellent communication skills; verbal, written and presentational. Excellent organisational skills and ability to maintain high performance. Experience in investigating, analysing, visualising, articulating and solving complex problems and concepts and make disciplined decisions based on available information. Excellent IT skills with proven ability to use and analyse data to support decision making and implement solutions. Degree in a science discipline or equivalent experience ideally with relevant project management qualifications. Person Specification: Method of assessment: A=Application, I=Interview, P=Presentation Behaviour Criteria: Delivering at Pace (A, I) Communicating and Influencing (A, I) Leadership (A, I) Experience Criteria: Experience in investigating, analysing, visualising, articulating and solving complex problems and concepts and make disciplined decisions based on available information (A, I, P) Evidence of working effectively as part of a multi-disciplinary team, working across boundaries and delegating where appropriate, adding value through strategic thinking (A, I, P) Strong customer service skills, with significant experience in communicating scientific and technical information effectively and building relationships with a wide range of stakeholders both internally and externally (A, I, P) Technical Criteria: Excellent IT skills with proven ability to use and analyse data to support decision making and implement solutions (A) Degree in a science discipline or appropriate work experience (A) Desirable qualifications and certifications: (A) - PRINCE2 Practitioner - Agile project management practitioner - APM Practitioner Qualification - APM Registered Project Professional Strengths Criteria Team Player (I) Explainer (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.uk The selection process: We 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. 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. In the instance that we receive a high number of applications, we will hold an initial sift based on the lead criteria of Experience in investigating, analysing, visualising, articulating and solving complex problems and concepts and make disciplined decisions based on available information and Degree in a science discipline or appropriate work experience. Use of AI in Job Applications Artificial 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 for more information on appropriate and inappropriate use. 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: 2nd February 2026 Shortlisting date: from 19th February 2026 Interview date: from 2nd March 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. 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. In 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, in the first instance, you should contact the MHRA Recruitment Team at careers@mhra.gov.uk. 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 About Us 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 agency is made up of c.1300 staff working across two main centres and peripatetically across the UK and abroad. The agency consists of Corporate, Digital & Technology, Enablement, Healthcare Quality & Access, Partnerships, Safety & Surveillance and Scientific Research & Innovation.

Responsibilities

The Platform Delivery Lead will drive the collaborative development and implementation of a modernised clinical trial application service in partnership with the Health Research Authority. This role is critical for enhancing the UK's reputation in clinical research and improving processes related to clinical trial assessments.