About CMR Surgical

At CMR Surgical, we're revolutionising the future of minimal access surgery with Versius, our next-generation surgical robotic system. We're growing fast, and we’re on a mission to transform how surgery is delivered globally—for the benefit of patients, clinicians, and healthcare systems.

Our values—Ambitious, Humble, People-Focused, and Fair & Responsible—define our approach to innovation, partnership, and growth. If you believe in making a meaningful difference in healthcare and want to be part of a purpose-driven company with bold ambitions, now is the time to join us.

CMR is an exciting and evolving company to be joining right now.  Our commitment to our goal of building a world-class medical devices company is underpinned by the ground-breaking innovation of our next generation of surgical robots and a diverse team of talented and supportive individuals.

We’re breaking new ground which makes working here exciting, it provides autonomy, opportunity and makes the things you do visible. Come and join us and see what you’re capable of.

About the Role

As a Clinical Trial Coordinator, you will be contributing to CMR Surgical by providing key support in the planning, execution, and management of clinical trials regarding the safe and effective use of Versius in patients. You will be part of the team that handles all clinical and pre-clinical studies including pilot, pivotal, and post-market studies.

Responsibilities

• Coordinate study start-up activities such as regulatory/ethics submissions as well drafting and organisation of trial documents
• Manage ongoing clinical trials, overseeing day-to-day study progress to ensure adherence to protocol, GCP, and regulatory standards
• Prepare and monitor study budget
• Support managing and updating internal and external stakeholders
• Serve as the central communication point between CMR, sites, and CROs
• Help develop study timelines and coordinate actions between various teams within CMR needed to ensure study success
• Facilitate study logistics such as device shipment, case support, and study payments
• Maintain trial master files (TMFs) ensuring completeness and quality throughout the study

We’d expect you to be willing to turn your hand to anything within the remit that helps the team deliver its objectives.

About You

To be successful in this role, you'll need to have/be:

• Batchelor's degree in relevant discipline, or equivalent
• Experience in clinical research coordination including aiding successful delivery of clinical trials (in academia or industry) mandatory
• Previous experience working with CRO, clinical sites and regulatory bodies
• Previous MedTech industry experience preferable
• Knowledge of GCP and clinical trial regulatory guidelines such as ISO-14155
• Strong organizational and project management skills
• Excellent communication and ability to work well in a team

Why Join Us?

We offer a competitive salary and a great benefits package including a bonus, non-contributory pension, provate healthcare, generous annual leave allowance and enhanced global parental leave pay.

This role requires candidates to have eligibility to work within the UK.

Interested? We’d love to hear from you!

Strictly no agencies?