Clinical Trial Manager

i-Pharm Consulting; Uxbridge; Hybrid; GBP 50,000 - 70,000; Full time

Job summary

A leading biopharma company is seeking a Clinical Trials Manager in Uxbridge, London, to oversee Phase Ib–III studies across EMEA. The ideal candidate will have a life science degree, substantial clinical trial management experience, and strong organizational skills. This role offers the chance to work on impactful virology research and a competitive package.

Benefits

Competitive package

Opportunities for growth

Supportive team culture

Qualifications

• Proven experience in clinical trial management at Sr CTMA level or higher.
• Co-monitoring and CRO/vendor oversight experience.
• Knowledge of ICH and EU/FDA regulations.

Responsibilities

• Manage regional activities of global Phase Ib–III virology trials.
• Coordinate with CROs and vendors throughout the study lifecycle.
• Support study documentation, timelines, and budgets.

Skills

Clinical trial management

GCP knowledge

Excellent organisational skills

Communication skills

Education

Life science degree or nursing qualification (BSc or equivalent)

Job description

Job Title: Clinical Trials Manager

Work location: Uxbridge, London, UK

Work structure: Monday to Friday, 37.5H/W. 3-5 days onsite

Contract duration: 12-months

About the Role

Are you a proactive Clinical Trial Manager with experience in global studies? Our client, a leading biopharma company, is looking for a talented CTM to join their team and manage Phase Ib–III studies across the EMEA region. This is a fantastic opportunity to contribute to impactful virology research within a collaborative, fast-paced environment.

Key Responsibilities

• Manage regional activities of global Phase Ib–III virology trials
• Coordinate with CROs and vendors throughout the study lifecycle
• Support study documentation, timelines, and budgets
• Oversee site readiness, monitoring, and compliance activities
• Provide country-specific regulatory and site feasibility insight
• Support study team communications and problem-solving

About You

• Life science degree or nursing qualification (BSc or equivalent)
• Proven experience in clinical trial management (Sr CTMA level or higher)
• Co-monitoring and CRO/vendor oversight experience
• Knowledge of GCP, ICH, EU/FDA regulations
• Excellent organisational and communication skills
• Virology experience is a plus, but not essential

What’s in it for you?

• Work on high-impact studies with a global footprint
• Collaborate with experts in a supportive team culture
• Gain exposure to strategic projects and international operations
• Competitive package and opportunities for growth

If you're ready to step into a high-visibility role that blends scientific impact with operational leadership, we’d love to hear from you.

Apply now to make your mark in virology research.

How to Apply:

To apply, please submit your CV outlining your qualifications and experience relevant to this role.

Please note: You must be able to work in the UK without restriction or sponsorship to be eligible for this role. If you are interested in finding out more about this role or others, please contact Jada Kirlew at [e-mail] or call: [phone] (UK) / [phone] (NL)