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- Tasks: Coordinate and manage clinical trials for innovative surgical technology.
- Company: Join CMR Surgical, a leader in minimal access surgery innovation.
- Benefits: Competitive salary, bonus, private healthcare, and generous leave.
- Why this job: Make a real impact in healthcare with cutting-edge robotic systems.
- Qualifications: Experience in clinical research and strong project management skills.
- Other info: Dynamic team environment with opportunities for personal and professional growth.
The predicted salary is between 36000 - 60000 £ per year.
At CMR Surgical, we are revolutionising the future of minimal access surgery with Versius, our next-generation surgical robotic system. We are 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.
As a Clinical Trial Coordinator / Study Manager, 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:
- 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
We offer a competitive salary and a great benefits package including a bonus, non-contributory pension, private healthcare, generous annual leave allowance and enhanced global parental leave pay. This role requires candidates to have eligibility to work within the UK.
Clinical Trial Coordinator / Study Manager in Cambridge employer: Cmr Surgical
Contact Detail:
Cmr Surgical Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Coordinator / Study Manager in Cambridge
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream role.
✨Tip Number 2
Prepare for interviews by researching CMR Surgical and our innovative work with Versius. Show us you’re passionate about minimal access surgery and how your skills align with our mission. We love candidates who are genuinely excited about what we do!
✨Tip Number 3
Practice your responses to common interview questions, especially those related to clinical trial management. We want to see how you handle challenges and your approach to teamwork—so be ready to share specific examples from your experience.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows us you’re serious about joining our team and contributing to our exciting journey in healthcare.
We think you need these skills to ace Clinical Trial Coordinator / Study Manager in Cambridge
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that align with the Clinical Trial Coordinator role. Highlight any relevant clinical research coordination experience and showcase your understanding of GCP and regulatory guidelines.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your passion for transforming healthcare and how your background makes you a perfect fit for CMR Surgical. Don’t forget to mention our values and how they resonate with you.
Showcase Your Team Spirit: We’re all about collaboration at CMR, so make sure to highlight your ability to work well in a team. Share examples of how you’ve successfully communicated and coordinated with various stakeholders in past roles.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands and shows your enthusiasm for joining our mission to revolutionise surgery!
How to prepare for a job interview at Cmr Surgical
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical trials and the specific role of a Clinical Trial Coordinator. Familiarise yourself with CMR Surgical's mission and values, especially their focus on innovation and patient care. This will show that you're genuinely interested in the company and its goals.
✨Showcase Your Experience
Prepare to discuss your previous experience in clinical research coordination. Be ready to share specific examples of how you've successfully managed trials, worked with CROs, or navigated regulatory submissions. Highlighting your hands-on experience will demonstrate your capability for the role.
✨Communicate Clearly
Since communication is key in this role, practice articulating your thoughts clearly and concisely. Think about how you can convey complex information simply, as you'll need to liaise with various stakeholders. A mock interview with a friend can help you refine your delivery.
✨Ask Insightful Questions
Prepare some thoughtful questions to ask at the end of your interview. Inquire about the team dynamics, the challenges they face in clinical trials, or how they measure success. This not only shows your interest but also helps you gauge if the company culture aligns with your values.