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Clinical trial manager

Uxbridge
R&D Partners
Clinical trial manager
Posted: 17 November
Offer 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. If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page. R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.r-dpartners.com/privacy-policy/

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