Clinical Study Manager
- Sponsor Dedicated
- Spain, UK, Romania, Bulgaria, Czech Republic
- remote Asegúrese de presentar su candidatura con toda la información solicitada, tal como se expone en la

descripción del puesto
a continuación. At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As a Clinical Study Manager at ICON being assigned to a single sponsor as a Biosamples Study Manager, you will support the successful delivery of clinical studies through oversight of biosample management activities, laboratory operations, and vendor partnerships. Your focus will be on coordinating clinical trial delivery, overseeing biosample management activities, resolving issues, and driving operational excellence across studies. Oversee the planning, execution, and monitoring of clinical studies to ensure compliance with regulatory requirements, study objectives, and project timelines. Lead oversight of biosample management activities, ensuring sample collection, processing, storage, shipment, tracking, and reconciliation activities are managed in accordance with protocol requirements and applicable regulations. Manage central laboratory and specialty vendor activities, including operational oversight, issue escalation, performance monitoring, and risk mitigation. Review and support the development of laboratory manuals, sample management plans, and study-specific laboratory procedures. Monitor sample traceability, chain-of-custody processes, and sample quality metrics throughout the study lifecycle. Develop and manage study budgets, resources, and timelines, ensuring efficient use of resources and adherence to study plans. Ensure data integrity and quality through effective oversight, monitoring, and compliance processes across all study activities. Support laboratory and biosample-related training and guidance for study teams and sites as required.



You will have solid clinical trial management experience combined with exposure to biosample management, laboratory operations, or central laboratory oversight within a clinical research environment. Bachelor's degree in a relevant scientific discipline or healthcare-related field. Proven experience in clinical study management with a strong understanding of the drug development process and regulatory requirements. Experience supporting biosample management activities within clinical trials, including oversight of sample collection, processing, storage, shipment, tracking, and reconciliation processes. Knowledge of laboratory manuals, sample management plans, sample traceability, and chain-of-custody processes. Strong project management skills, including the ability to manage multiple priorities and stakeholders simultaneously. Detail-oriented with focus on quality, compliance, and operational excellence. Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. A range of health insurance offerings to suit you and your family's needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. Versátil country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. xohynlm All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

📌 Senior Clinical Study Manager (España)
🏢 Icon Clinical Research
📍 España