Senior Programme Coordinator

3 weeks ago


London, Greater London, United Kingdom Medicines and Healthcare Products Regulatory Agency Full time

Position Overview

We are seeking a Programme Manager to oversee initiatives within our Innovation Accelerator division, part of the Science, Research & Innovation sector.

This is a full-time role on a fixed-term contract basis, with potential for extension. The position will require a presence in the UK, adhering to the agency's policy of in-office collaboration.

Government entities are striving for a minimum of 60% in-office attendance to enhance teamwork and stakeholder engagement.

We are adopting a flexible, hybrid working model, with a minimum of 8 days per month required on-site to facilitate essential interactions with partners and stakeholders. Depending on business requirements, this may increase to 12 days monthly, with the remaining time allocated for remote work or office presence. Certain roles may necessitate more frequent on-site attendance.

About Us

The Medicines and Healthcare products Regulatory Agency is dedicated to improving public health through effective regulation of medicines and medical devices, supported by scientific research.

The Science, Research and Innovation Group is committed to delivering impactful public health outcomes, pioneering research, and a distinctive approach through a robust Science Strategy that balances innovation with sustainability and cost-effectiveness. This group is segmented into six sub-divisions, including Innovation Accelerator, Clinical Investigations and Trials, Research and Development, Standards Lifecycle, Control Testing and Quality Assurance, and Health & Safety.

The Innovation Accelerator (IA) connects innovators with the Agency’s scientific expertise and regulatory guidance, facilitating the development of cutting-edge products, including medicines and medical devices.

Role Responsibilities

The successful candidate will collaborate across the Agency and with key stakeholders in the UK health and care system to implement the Innovative Devices Access Pathway (IDAP). The objective of IDAP is to enhance patient access to innovative medical technologies and devices that fulfill unmet clinical needs by providing developers with coordinated guidance to ensure the generation of suitable evidence for regulatory approval and health economic evaluations. This role presents a unique opportunity to be at the forefront of medical device innovation in the UK.

Key Duties:

  • Utilize programme management expertise to design, execute, and monitor the Innovative Devices Access Pathway (IDAP) and its integration with the Innovative Licensing and Access Pathway (ILAP).
  • Contribute to the establishment and management of governance and procedural frameworks for IDAP and ILAP projects, defining operational roles and responsibilities.
  • Define and uphold project management standards across the portfolio in alignment with the Agency’s Strategic Change Assurance Office structure.
  • Provide line management to the project team as necessary.

Candidate Profile

The ideal candidate will possess:

  • Proven experience in managing complex programmes involving multiple stakeholders.
  • Experience in a medical, scientific, or healthcare setting is preferred.
  • Management experience, either direct or in a matrix environment.
  • Relevant qualifications in programme management, such as Prince 2 or Programme Management Professional.
  • A bachelor’s degree in a scientific discipline is desirable.

Benefits

In addition to a competitive salary, the Medicines and Healthcare Products Regulatory Agency offers a comprehensive benefits package, including contributions towards a Civil Service Defined Benefit Pension scheme, annual leave, occupational sick pay, and opportunities for ongoing learning and development.



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