CPRD IR Researcher

Company: MHRA

Location: London

Posted: May 8th, 2026

We are currently looking for an IR Researcher to join our Clinical Practice Research Datalink team in the Safety and Surveillance 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. Please note that this role can only be worked in the UK and not overseas.

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 on site to enable collaboration and contact with partners and stakeholders. Attendance on site may flex up to 12 days a month depending on business needs.

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 Safety and Surveillance Group brings together devices and medicines safety expertise with enforcement capabilities. The Clinical Practice Research Datalink (CPRD), with support from NIHR, is the UK’s pre‑eminent research service providing access to anonymised NHS data for research.

What’s the role?

The CPRD Researcher will apply their epidemiological, statistical, data management and data analysis expertise to further public health research. The post holder will undertake internal development, collaborative research and use CPRD data to support interventional research. The role will also involve input into the development and application of best practice that contribute to the maintenance of CPRD as a centre of excellence for observational and interventional research using the primary care database.

We are seeking a motivated individual who has experience in epidemiology, statistics and outcomes research or public health research. The post holder will have excellent organisational, analytical and communication skills, take a thorough and rigorous approach to quality assurance, and have the determination and ability to work independently.

Key responsibilities

Who are we looking for?

#J-18808-Ljbffr
Apply Now