Experteer Overview La información a continuación detalla los requisitos del puesto, la experiencia esperada del candidato y las cualificaciones correspondientes. In this Sr CTM role, you will oversee site management, clinical monitoring, and central monitoring to ensure patient safety, data integrity, and GCP/compliance. You will coordinate with cross-functional teams to hit milestones, manage risks, and optimize study delivery in a general, fast-paced environment. The position supports both Functional Service Provider partnerships and Full-Service settings, contributing to the company’s mission of accelerating patient progress. You will lead and mentor clinical trial teams, shaping trial execution and quality. This is an opportunity to drive impactful clinical delivery within a world-class life sciences organization.Compensaciones / Beneficios• Oversee site management and monitoring deliverables from activation to closeout with focus on patient safety and data integrity• Review study scope, budget, and protocol content; align CRA/CeM activities with contractual obligations• Identify risks to trial deliverables and escalate as needed; propose mitigations• Represent the team in key meetings and act as escalation point for investigator interactions• Collaborate with other functional leaders to coordinate handoffs and meet milestones (site activation, enrollment,



database lock)• Develop and maintain clinical study tools and templates (e.g., Clinical Monitoring Plan); ensure CTMS and dashboards are usable and auditable• Coordinate training for study team on protocols, CRFs, SOPs, data plans, and timelines• Oversee resourcing, site assignments, and conduct to ensure quality and on-time delivery• Monitor and review CTMS, EDC, eDiary, ePRO, TMF, IVRS/IWRS dashboards to reflect operational progress• Ensure compliance with monitoring strategy, CMP/SMP, and risk plans; contribute to risk assessment plans• Provide client updates on deliverables and risks; propose solutions for protocol execution obstacles• Mentor and coach CTMs and possibly coordinate larger teams across portfoliosResponsabilidades• Bachelor's xcskxlj degree or RN in related field; equivalent experience• Proven ability to lead teams toward milestones and operate in international settings• Expertise in site management and monitoring (clinical or central)• Knowledge of GCP/ICH and regulatory requirements• Strong computer skills and ability to manage budgets and timelines• Excellent conflict resolution and problem-solving abilities• Ability to travel ~20%• Experience with risk-based monitoring is preferredRequisitos principales• career development• supportive and engaged line management• inclusive culture• peer recognition• total rewards program• global collaboration

📌 Sr CTM. Location: Barcelona or Madrid. FSP Sponsor dedicated.
🏢 Talent
📍 Madrid