Overview In this role you will oversee site management, clinical and central monitoring to safeguard patient safety, data integrity, and regulatory compliance. You will manage activities from activation to closeout, coordinate with cross-functional teams, and apply risk-based approaches to keep trials on track. You will engage with investigators and sites, support study budgets and timelines, and contribute to inspection readiness. This position offers remote work in the UK, Poland, Spain, or Bulgaria within a large, mission-driven organization.

Compensaciones / Beneficioscareer development and progressioninclusive culturesupportive line managementtechnical and therapeutic area trainingpeer recognitiontotal rewards program ResponsabilidadesOversee site management, monitoring and central monitoring deliverables with focus on patient safety and data integrityManage site interactions from activation through closeout, including recruitment and investigator payments as neededIdentify risks to delivery using operational data and escalate to project manager when necessaryCollaborate with Study Start Up, Patient Recruitment and Data Management to hit milestones (activation, enrollment, database lock)Develop and maintain clinical study tools (e.g., Clinical Monitoring Plan)



and ensure CTMS and dashboards are usableCoordinate training for study team on protocols, CRF completion, SOPs, data plans and timelinesOversee resource allocations for CRAs and Central Monitors, monitor team conduct and risk to deliveryReview and provide feedback on functional plans and ensure quality of monitoring and site management deliverablesInteract with clients and cross-functional departments to report status and resolve protocol execution obstaclesSupport inspection readiness and develop corrective action plans as neededProvide performance feedback to line managers and support larger, more complex trials Requisitos principalesBachelor’s degree or RN in a related field or equivalent combination of education, training and experienceDemonstrated ability to lead and align teams to milestonesExperience in international environments and in site management/monitoringKnowledge of GCP/ICH guidelines and regulatory requirementsStrong communication, presentation and interpersonal skillsGood computer skills and familiarity with trial systemsAbility to apply risk management and problem solving to clinical trialsModerate travel (~20%)strong communicationconflict resolutionproblem solvingCTMSEDCeDiary

📌 Single Sponsor Global Clinical Trial Manager II (Solid CRA background) fully home based in UK, Polan (Madrid)
🏢 Jobrapido
📍 Madrid