Manager, Clinical Trial Operations

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Manager, Clinical Trial Operations, Hampshire

Client:

Carrot Recruitment

Location:

Hampshire, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

8

Posted:

18.04.2025

Expiry Date:

02.06.2025

Job Description:

Manager, Clinical Trial Operations - Hampshire – Medical Devices – Competitive Salary and Package

The Company

Carrot Recruitment is working with a global medical device company seeking a highly motivated and experienced Manager of Clinical Trials Operations to manage a dynamic team with both hands-on trial management and leadership experience. The ideal candidate will have a strong background in clinical research and management, focusing on overseeing the execution of clinical trials and ensuring compliance with regulations and protocols for medical devices.

The Role

• 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.

You

• Bachelor's degree in a scientific or healthcare-related field; advanced degree preferred.
• Seasoned professional within clinical research, with extensive medical device exposure and expertise in clinical trial management, including protocol development, site selection, and monitoring (Ophthalmology experience desirable).
• Leadership and 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 setup and management of post-market clinical follow-up (PMCF) studies.

What should you do next?

This role is one not to be missed; it encompasses the opportunity to work with an established medical device company with a global presence committed to employees' personal and professional development.

To discuss this role further or to find out about other roles I’m currently working on, please get in touch or hit apply to submit your current CV.

Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are already authorized 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, color, 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.