Clinical Trial Manager

R&D Partners; City Of London; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading pharmaceutical firm in Uxbridge is hiring a Clinical Trial Manager to oversee regional management of Phase Ib-III studies across the EMEA region. The role requires organizing and coordinating efforts among cross-functional teams while ensuring compliance with regulatory standards. Ideal candidates will have a scientific degree and significant study management experience, along with strong communication and organizational skills. International travel may be required.

Qualifications

• Significant relevant experience in a scientific discipline.
• Previous study management/coordination experience at a Senior CTMA level.
• Monitoring experience is highly desirable.
• Knowledge of Virology is advantageous but not essential.

Responsibilities

• Provide regional management of global Phase Ib-III studies.
• Draft and coordinate the review of study documents.
• Maintain study timelines and contribute to budget development.
• Manage CROs/vendors and oversee site budget/contract processes.
• Coordinate data review and preparation of reports.

Skills

Organizational skills

Communication skills

Problem-solving abilities

Teamwork

Decision-making

Learning agility

Education

BSc or nursing qualification

Job description

Lead the future of global clinical trials-drive innovation, collaboration, and impact across EMEA.

R&D Partners is seeking a Clinical Trial Manager to join a leading pharmaceutical company in Uxbridge, UK. This role focuses on regional management of Phase Ib-III clinical studies, with a strong emphasis on the EMEA region. The successful candidate will work as part of a Global Study Team under the guidance of a Clinical Program Manager, contributing to all stages of clinical trials from start-up to close-out.

This position requires a collaborative individual with excellent organizational and communication skills, capable of managing stakeholders and working across cross-functional teams globally.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities

• Provide regional management of global Phase Ib-III studies.
• Draft and coordinate the review of study documents (protocols, informed consents, case report forms, monitoring plans, etc.).
• Maintain study timelines and contribute to budget development.
• Manage CROs/vendors and oversee site budget/contract processes.
• Coordinate data review and preparation of interim/final clinical study reports.
• Train CROs, vendors, investigators, and study coordinators on study requirements.
• Conduct monitoring/co-monitoring as required.
• Collaborate with local medical affairs colleagues on country‑specific studies and initiatives.
• Ensure compliance with FDA, EU Regulations, ICH Guidelines, and GCPs.
• Serve as a resource for clinical trial management expertise within the company.
• Contribute to Clinical Operations International team activities and initiatives.

Key Skills and Requirements

• Significant relevant experience and a BSc or nursing qualification in a scientific discipline.
• Previous study management/coordination experience at a Senior CTMA level.
• Monitoring experience is highly desirable.
• Knowledge of Virology is advantageous but not essential.
• Thorough understanding of FDA/EU Regulations, ICH Guidelines, and GCPs.
• Strong organizational, decision‑making, and teamwork skills.
• Ability to prioritize multiple tasks and adapt to changes.
• Excellent communication skills and problem‑solving abilities.
• Willingness to travel internationally as required.

Behaviors and Core Values

• Curious with strong learning agility.
• Operationally excellent and resilient in a dynamic environment.
• Organized with a systematic approach to prioritization.
• Exhibits core values of integrity, teamwork, excellence, accountability, and inclusion.

For more information, please contact Athi Singata.

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