Senior Clinical Scientist

Were 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 SurgicalCMR 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 JobAs 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 & ResponsibilitiesDraft clinical trial protocols, informed consent forms, and investigator brochuresHelp manage ongoing clinical trials through data monitoring, safety reporting, and coordinating with site study teams and/or CROsContribute to interpretation of trial results and draft clinical trial reportsLead critical assessment of scientific literature including targeted and systematic reviewsSupport the team in design and execution of pre-clinical studiesSupport regulatory submissions and post-market surveillance activitiesWed expect you to be willing to turn your hand to anything within the remit that helps the team deliver its objectives.Knowledge and Skills requiredExperience working as a scientist in clinical research including successful delivery of clinical trials (in academia or industry) mandatoryDeep understanding of trial methodology, design, and regulationsExperience in design, documentation, data management, and interpretation of clinical trials resultsUnderstanding of research science and product development processesGood communication and ability to work well in a teamQualifications and ExperienceMasters or PhD degree in a relevant disciplinePrevious MedTech industry experiencePractical understanding of ICH-GCP and clinical trial regulationsPractical understanding of ISO-14155Why 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? Wed love to hear from you!This role requires candidates to have eligibility to work within the UK.Strictly no agencies#LI-Hybrid

Created: 2025-12-12