Clinical Scientist / Senior Clinical Scientist - #150520

We’re looking for an exceptional 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.

As a 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.

About CMR Surgical

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.

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’re a rapidly developing company and roles can change and evolve. You’ll be willing to turn your hand to anything within the Clinical remit that supports the team with delivering its objectives.

About You

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

• Experience in clinical research including successful delivery of clinical trials 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
• Master’s or PhD degree in a relevant discipline
• Previous MedTech industry experience, or equivalent
• Practical understanding of ICH-GCP and clinical trial regulations
• Practical understanding of ISO-14155

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.

We’d really like to hear from applicants from underrepresented groups and we recognise everyone has individual personal circumstances, so we’re open to discussing reduced / flexible / hybrid working hours for this role.

Why Join Us?

We offer a competitive salary and a great benefits package including a bonus, non-contributory pension, private healthcare which covers pre-existing conditions, annual personal day for every employee to use however they wish and enhanced global parental leave pay.

We recognise that everyone has a life outside of work and at times we can experience things which are significant and can impact on our working lives. We’ve just launched our Global Parental Leave and Health and Wellbeing leave supporting our colleagues going through the menopause, fertility cycles or pregnancy loss and those going through gender reassignment; allowing them time to look after themselves and those close to them.

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.

Strictly no agencies