CPRD FTC Clinical Study Coordinator

The MHRA is transforming. Through enabling innovation, making the right judgements of the benefits and risks of medical products and forging the right partnerships in the UK and internationally, it aims to deliver world class regulation and improved outcomes for UK patients.

We currently have an exciting opportunity for a FTC Clinical Study Coordinator to join our Clinical Practice Research Datalink team in the Safety and Surveillance group.

Within a week of working here, your day could look like this: being responsible for supporting the delivery of the Interventional Research (IR) services within the growing portfolio of clinical trials, patient referral services and clinical surveys. The post holder will work closely with CPRD colleagues and regularly liaise with the study Sponsor team, study investigators and GP practice staff. We are seeking a responsible individual with experience working in a clinical operations or clinical research setting.

The successful candidate will Experience in contributing to the delivery of projects.  Experience of working in a clinical operations, health or clinical research role.

• Excellent administrative skills with experience of effectively maintaining records and information systems, providing regular progress updates against milestones and metrics.
• Take responsibility for making effective and fair decisions in a timely manner.
• Analyse and research further information to support decisions and talk to relevant people to get advice and information when unsure how to proceed.

Closing date: 19^th August 2024

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