Global Lead, Decentralized Clinical Trials

IQVIA; Madrid; Presencial; EUR 90.000 - 120.000; Jornada completa

Descripción de la vacante

IQVIA in Madrid is seeking a Decentralized Clinical Trial Study Lead (DCTL) to direct DCT studies from planning to delivery, coordinating with technology, site services, regulatory and IT teams. The role emphasizes strategic oversight, proactive issue resolution and maintaining project profitability.

The candidate must have a life sciences degree and at least 5 years in clinical research, with strong project management, leadership and regulatory know-how to drive successful, compliant trials.

Formación

• Requires 5 years relevant clinical research experience or equivalent combination of education, training and experience.
• Requires advanced knowledge of and experience implementing Project Management methodologies.
• Broad knowledge of DCT and related areas through education and experience.

Responsabilidades

• Oversee the strategic development and delivery of DCT studies within contract terms while optimizing speed, quality and cost.
• Serve as DCT project oversight contact with customers and own relationships with key customer contacts.
• Set objectives for the DCT project team and assess performance with leadership and feedback.
• Collaborate with core study teams to develop integrated study management plans and support milestones.

Conocimientos

Project management

Clinical research

Communication

Leadership

Cross-functional collaboration

Educación

Bachelor's Degree Life sciences or related field

Herramientas

MS Office

Descripción del empleo

IQVIA in Madrid is seeking a Decentralized Clinical Trial Study Lead (DCTL) to direct DCT studies from planning to delivery, coordinating with technology, site services, regulatory and IT teams. The role emphasizes strategic oversight, proactive issue resolution and maintaining project profitability.

The candidate must have a life sciences degree and at least 5 years in clinical research, with strong project management, leadership and regulatory know-how to drive successful, compliant trials.