Platform Delivery Lead

Job Category Administration / Corporate Support

• Posting Date 01/27/2026, 08:21 AM
• Apply Before 02/02/2026, 11:55 PM
• Grade SEO(I)
• Locations Agency HQ
• Contract Type Fixed Term - In
• Shortlisting Date from 19th February
• Interview Date from 2nd March

Overview

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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 31 st March 2027. The role will be based at 10 South Colonnade, Canary Wharf London, E14 4PU.

Government departments and agencies are moving toward a minimum 60% attendance in office sites. We are implementing a flexible, hybrid way of working, with a minimum of 8 days per month on site to enable collaboration with partners and stakeholders. The on-site requirement may rise to 12 days a month depending on business needs. Some roles may allow remote work; discuss with the recruiting manager before accepting an appointment.

Who we are

The Medicines and Healthcare products Regulatory Agency enhances and improves the health of millions of people daily through 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 Science Strategy balancing innovation with sustainability and affordability. It comprises 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 is instrumental in maintaining and enhancing the UK's reputation as a great place to conduct clinical research for medicines and devices. The role holder will drive collaboration with the HRA to develop an IT platform for a modernised end-to-end service of clinical trial applications, aiming to modernise processes, improve data use, increase automation, improve reporting, and support risk-proportionate decision-making in MHRA and NHS planning.

Key responsibilities

• Drive the collaborative development and implementation of a modernised end-to-end clinical trial application service in partnership with the Health Research Authority (HRA) and MHRA teams, aligning with the replacement of the Integrated Research Application System (IRAS) under the Research Systems Programme (RSP).
• Lead the modernisation of clinical trial processes, focusing on data utilisation, automation, and reporting to support risk-proportionate decision-making in line with MHRA and NHS 10-year Health Plan objectives.
• Lead the transition from IRAS and Appian systems, addressing integration challenges and minimising disruption through project planning and stakeholder engagement.
• Provide regular progress updates and analysis to senior management, highlighting risks, opportunities, and the impact of system changes on trial assessment efficiency and quality.

Who are we looking for?

Oursuccessful 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 to inform decisions.
• 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: Investigating, analysing, visualising, articulating and solving complex problems; working effectively in a multi-disciplinary team; strong customer service and ability to communicate scientific/technical information
• Technical Criteria: Excellent IT skills; degree in science or relevant work experience

Other information

Online application form questions based on Behaviour, Experience and Technical Success Profiles. Please ensure all questions are completed in full. Applications are CV blind.

Use of AI in Job Applications: AI can be a useful tool, but all examples must be truthful and from your own experience. See candidate guidance for more information.

If you require disability adjustments at any stage, please contact as soon as possible.

Closing date: 2 February 2026. Shortlisting: from 19 February 2026. Interview: from 2 March 2026.

For assistance applying or questions, please contact .

Candidates will be subject to UK immigration and Civil Service nationality rules. Further information is available here.

Successful candidates must pass security checks and may be subject to vaccinations or health surveillance as required by role. Some roles may require overseas travel.

Internal screening: applications may be checked against the Internal Fraud Database. A candidate is not eligible to apply if previously dismissed for fraud within a 5-year period.

Other information about government-wide schemes and childcare may apply where applicable.

The Medicines and Healthcare products Regulatory Agency is comprised of 1300 staff across two main centres and other sites, with teams across Corporate, Digital & Technology, Enablement, Healthcare Quality & Access, Partnerships, Safety & Surveillance, and Scientific Research & Innovation.