Clinical Research Associate

CMR Surgical; Cambridge; Hybrid; GBP 40,000 - 70,000; Full time

Job summary

An exciting opportunity awaits for a Clinical Research Associate in a forward-thinking medical devices company. This role is pivotal in managing clinical trials for an innovative surgical robotic system, focusing on both pre- and post-market studies. You will collaborate with a dynamic team, ensuring the safe and effective use of cutting-edge technology while contributing to the advancement of medical science. The company fosters an inclusive culture, promoting work-life balance and professional growth. If you are passionate about clinical research and eager to make a significant impact, this role is perfect for you.

Benefits

Competitive Salary

Bonus

Pension

Private Healthcare

Personal Days

Enhanced Parental Leave

Work-Life Balance Initiatives

Qualifications

• Extensive experience in clinical research as a sponsor.
• Knowledge of trial methodology, design, and regulations.
• Experience in developing case report forms.

Responsibilities

• Provide input to clinical trial protocols and data monitoring plans.
• Manage ongoing clinical trials through data monitoring and safety reporting.
• Contribute to data analysis and draft clinical trial reports.

Skills

Clinical Research Management

Data Collection

Safety Reporting

Clinical Data Analysis

Communication Skills

Problem-Solving Skills

Teamwork

Education

Bachelor's or Master's degree in a relevant discipline

Tools

Electronic Data Platforms

Data Analysis Tools

Microsoft Office

Job description

We’re looking for an exceptional Clinical Research Associate 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 execution and management of pre- and post-market clinical trials for Versius, our surgical robotic system. This role involves dynamic participation in all aspects of designing and running a clinical trial as a sponsor. 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 Research Associate, you will contribute 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 committed to building a world-class medical devices company. Our innovation in next-generation surgical robots is supported by a diverse team of talented individuals. Working here offers autonomy, opportunity, and visibility for your contributions. Join us and discover your potential.

Responsibilities

• Provide input to clinical trial protocols and data monitoring plans, review monitoring visit reports
• Identify, communicate, and mitigate risks in clinical data collection and monitoring
• Help create and manage investigator site files, trial master files, case report form templates, and electronic case report forms
• Manage ongoing clinical trials through data monitoring, safety reporting, and coordination with site study teams and CROs
• Contribute to data analysis, interpretation of trial results, and draft clinical trial reports
• Support regulatory submissions and post-market surveillance activities
• Assist in the assessment of scientific literature, including systematic reviews

Roles may evolve as the company develops, and flexibility within the clinical remit is encouraged to support team objectives.

About You

To succeed, you should have:

• Extensive experience in clinical research as a sponsor, including data collection, management, and safety reporting
• Experience in developing case report forms and using electronic data platforms
• Knowledge of trial methodology, design, and regulations
• Experience in clinical data analysis, interpretation, and presentation
• Understanding of research science and product development processes
• Good communication skills and teamwork ability
• Problem-solving skills and adaptability
• Bachelor’s or Master’s degree in a relevant discipline, or equivalent
• Previous MedTech industry or healthcare experience
• Proficiency in data analysis tools and Microsoft Office
• Knowledge of ICH-GCP and clinical trial regulations, including ISO-14155

We value diversity, inclusion, and authenticity. We welcome applicants from underrepresented groups and are open to flexible working arrangements. Our benefits include a competitive salary, bonus, pension, private healthcare, personal days, and enhanced parental leave. We support work-life balance and well-being initiatives.

Please submit a cover letter explaining your interest in CMR Surgical and providing an example of problem-solving in clinical trial management. Note: Eligibility to work in the UK is required. No agency applications accepted.