We’re looking for an exceptional Clinical Scientist or Senior Clinical Scientist to join our Medical Affairs Team, based in Cambridge, and reporting to our Clinical Research Lead. 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 our Cambridge office. 

About CMR Surgical

CMR is an exciting and evolving company to be joining right now. Our commitment to 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.

Purpose of Job:

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.

Specific Role & 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.

Knowledge and Skills required:

• 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
• 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

  Qualifications and Experience:

• Master’s or PhD degree in a relevant discipline
• Previous MedTech industry experience
• Practical understanding of ICH-GCP and clinical trial regulations
• Practical understanding of ISO-14155

Why Join Us?

We offer a competitive salary and a great benefits package including a bonus, pension, healthcare, annual personal day for every employee to use however they wish and enhanced global parental leave pay. 

CMR can support with travel reimbursement for in-person interviews if you need a taxi for access needs. 

Interested? We’d love to hear from you!

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

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