Clinical Trial Manager

JR United Kingdom; England; Hybrid; GBP 45,000 - 65,000; Full time

Job summary

A leading medical device company in the UK is seeking a Clinical Trials Manager to lead clinical studies with full autonomy. This role offers the chance to shape trial processes in a supportive environment, ideal for someone with prior clinical trials experience in medical devices. Join a growing organization focused on innovative healthcare solutions and enjoy hybrid working with travel to research sites.

Qualifications

• Must have prior experience working on clinical trials for medical devices.
• Ready for greater ownership in clinical trial management.
• Confident working with minimal internal support.

Responsibilities

• Designing and managing clinical studies.
• Writing protocols and Clinical Investigation Plans.
• Ensuring alignment with ICH-GCP and UK/EU regulations.

Skills

Clinical trial management

Protocol development

Regulatory compliance

Cross-functional collaboration

Job description

Clinical Trials Manager – Medical Devices

Hybrid (UK-Based – Commutable to Southern UK Research Sites)

Take the Lead in a High-Ownership Role

My client is a small, UK-based medical device company developing Class II technologies. With strong clinical foundations, in-house research capability, and a human-focused mission, they’re hiring a Clinical Trials Manager to lead the design, delivery, and oversight of clinical studies.

This is a newly created role with full autonomy across the clinical trial lifecycle. You’ll be the go-to person for protocol development, monitoring oversight, and evidence generation — ideal for someone confident working independently within a supportive, fast-moving team.

Location & Flexibility

Hybrid working, with regular travel to multicentre UK research sites. Best suited to someone based within reach of southern UK research hubs, with flexibility to be on-site when needed.

Why This Role?

• Join a company with in-house research infrastructure and thousands of treatments already delivered
• Work in a regulated, ISO-certified environment where clinical rigour is matched by agile delivery
• Contribute to a fast-growing organisation that’s expanded significantly in the past two years
• Be part of a small, close-knit team with direct access to decision-makers
• Shape how trials are run and build out the clinical function alongside experienced internal stakeholders
• Play a key role in a mission-led company focused on empowering people through meaningful innovation

What You’ll Be Doing

• Designing and managing clinical studies
• Writing protocols, Clinical Investigation Plans, and submission documents
• Managing site setup, monitoring, and compliance
• Ensuring alignment with ICH-GCP and UK/EU regulations
• Collaborating cross-functionally with clinical, regulatory, and product teams
• Leading internal staff and managing day-to-day operational delivery

Who This Might Suit

• A Clinical Trials Manager or Clinical Project Manager ready for greater ownership
• An experienced Associate CTM ready to step up and lead trials end-to-end
• Someone confident working with minimal internal support, across both strategic and operational responsibilities
• Must have prior experience working on clinical trials for medical devices

Interested?

If you’re ready to lead trials with autonomy and impact — and are based within reach of southern UK research centres — apply today or contact [e-mail]

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Created on 23/05/2025 by JR United Kingdom