Senior Clinical Scientist

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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 Senior Clinical Scientist, you will be contributing to CMR Surgical by providing clinical evidence 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. This position will play a crucial role in the design and execution of pre- and post-market clinical trials for Versius, our surgical robotic system.

This role is offered on a hybrid basis, with a minimum of 3 days a week being based in the office.

The job title for this role is to be finalised. If this remains as Senior Clinical Scientist Health & Care Professions Council (HCPC) membership will be required. This can be discussed during the application process.

Responsibilities

• Draft clinical trial protocols, informed consent forms, and investigator brochures
• Help manage ongoing clinical trials through data monitoring, safety reporting, and coordinating with site study teams and/or CROs
• Contribute to interpretation of trial results and draft clinical trial reports
• Lead critical assessment of scientific literature including targeted and systematic reviews
• Support the team in design and execution of pre-clinical studies
• Support regulatory submissions and post-market surveillance activities

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:

• Master's or PhD degree in a relevant discipline
• Experience working as a scientist in clinical research including successful delivery of clinical trials (in academia or industry) mandatory
• Deep understanding of trial methodology, design, and regulations including ICH-GCP and ISO-14155
• Experience in design, documentation, data management, and interpretation of clinical trials results
• Understanding of research science and product development processes
• Good communication and ability to work well in a team

At CMR we're building a diverse, inclusive, and authentic workplace; what matters most to us is that you identify with our values and are passionate about making a difference.

Why Join Us?

We offer a competitive salary and a great benefits package including a bonus, pension, healthcare and enhanced global parental leave pay.

Interested? We'd love to hear from you!

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

Strictly no agencies