Overview As a Senior Clinical Trial Manager, you will oversee site management, monitoring, and data integrity for oncology trials from a home base in Spain. You’ll coordinate a cross-functional clinical team to achieve study milestones, manage risks, and ensure protocol and regulatory compliance. You’ll act as a key liaison with investigators, sites, and sponsors, driving quality and delivery while supporting inspections readiness. This role offers impact across the drug development continuum, with opportunities to shape trial delivery and processes in a fast-paced, inclusive environment.

Compensaciones / Beneficioscareer developmentinclusive culturetotal rewards programtechnical and therapeutic area training ResponsabilidadesOversee site management, clinical/central monitoring deliverables with emphasis on patient safety and data integrityManage site interactions from activation to closeout, including recruitment and investigator paymentsIdentify and mitigate risks using data, escalating issues to project management as neededCoordinate and review study scope, budget, and protocol content to align with contractual obligationsLead and participate in key meetings (e.g., Kick Off) and provide status updates on deliverables and risksDevelop and maintain study tools/templates (e.g., Clinical Monitoring Plan) and ensure CTMS and dashboards are usableProvide initial and ongoing training to study teams on protocols, CRFs, SOPs,



data plans, and timelinesOversee resourcing allocations for CRAs and Central Monitors and monitor team conduct and delivery qualityReview monitoring documentation and ensure timely updates in CTMS and other systemsInteract with client and other functions to resolve obstacles and ensure compliance with protocol and regulatory requirementsSupport inspections readiness and implement corrective action plans as neededMentor and coach CTMs on clinical delivery, risk assessment, and action implementationMay coordinate activities across a portfolio of projects or larger, more complex trials Requisitos principalesBachelor’s degree or RN in a related field or equivalentProven vendor management experienceGlobal study management experienceExperience in Oncology clinical trialsStrong experience reviewing and overseeing study plans and documentationAbility to lead and align teams to milestonesExperience in international environmentsExpertise in site management and monitoring (clinical or central)Knowledge of risk-based monitoring (preferred)Budget management and understanding of clinical trial financial principlesKnowledge of GCP/ICH and regulatory requirementsStrong computer and data skills; conflict resolution and problem-solving abilitiesWillingness to travel ~20%leadershipcommunicationproblem solvingCTMSEDCeDiary

📌 Global Sr CTM - Home Based in SPAIN. FSP. Oncology experience is required.. (Madrid)
🏢 Jobrapido
📍 Madrid