Manager, Clinical Trial Operations

Are you a seasoned Clinical Operations professional within the medical device space?

Carrot Recruitment are working with a Global Medical Device company seeking a highly motivated and experienced Manager of Clinical Trials Operations to manage a dynamic team. The successful individual must have both hands-on trial management and leadership experience to work in the UK based Clinical Operations team specifically within medical devices for this on-site position.

Everything you need to know about the role 

As manager to a small UK team, you will have a strong background in clinical research and management, with a focus on overseeing the execution of clinical trials and ensuring compliance with regulations and protocols for medical devices. You will work closely with US counter parts and the Global Clinical Operations division to support the completion of post market clinical studies.

 Further to this you will:

• Oversee and manage the planning and execution of PMCF studies, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements
• Lead a team of Clinical Research Associates (CRAs)
• Collaborate with cross-functional teams to develop and implement clinical trial protocols, informed consent forms, and other study-related documents.
• Monitor and track study progress, including patient recruitment, data collection, and monitoring activities.
• Manage trial budgets, timelines, and resource allocation to ensure successful trial completion.
• Serve as the primary point of contact for study sponsors, investigators, and other stakeholders.

Experience and qualities that make you a strong fit

• Bachelor's degree in a scientific or healthcare-related field; advanced degree preferred.
• Seasoned professional within clinical research, with extensive medical device exposure with expertise in clinical trial management, including protocol development, site selection, and monitoring (Ophthalmology experience desirable)
• Leadership/management experience with excellent communication skills and the ability to effectively mentor and motivate team members.
• Knowledge of regional regulatory requirements (UK&EU), GCP, and ICH guidelines. (Experience of Regulatory submission advantageous)
• Experience in the set up and management of post market clinical follow-up (PMCF) studies
• Vendor management (CRO oversight) experience

What’s on offer?

• A competitive base salary
• Annual leave of 25 days plus bank holidays
• 10% bonus
• Private medical
• Pension scheme
• Healthcare cover
• Life assurance
• Access to a Wellness Platform to support you in mental health and wellbeing

Could this be the role for you?

If you’re ready to take on this exciting opportunity and bring your expertise to a company with a global reach, we’d love to hear from you.

Please apply below or send your CV and a brief cover letter to [email protected]

Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are already authorised to work there.
Carrot Recruitment acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and/or expression.
If there are any arrangements or adjustments we can make to assist you at interview then please let us know and we’ll be more than happy to assist.