Director, Clinical Project Delivery (MASH)

IQVIA

Madrid

Presencial

EUR 108.000 - 302.000

Jornada completa

Hace 9 días
Generador de candidaturas

Una candidatura hecha para este puesto de trabajo: un currículum y una carta de presentación adaptados que responden directamente a la oferta.

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Descripción de la vacante

IQVIA is seeking a Clinical Project Management Director in Madrid to lead a team responsible for the clinical delivery of complex, multi-regional studies and programs. You will drive strategic decision-making, ensure on-time, high-quality delivery, and manage financial performance and customer satisfaction.

The role requires seasoned leadership with strong communication and collaboration skills, and a deep understanding of clinical trial conduct and regulatory requirements.

Formación

  • Bachelor’s Degree in Life sciences or related field.
  • Extensive knowledge of multiple job areas through education and experience.
  • Strong command of English and excellent written/verbal communication.

Responsabilidades

  • Develop the project delivery strategy for RFPs and lead bid defense presentations.
  • Oversee integrated study management plans with the core project team.
  • Direct the execution of clinical studies ensuring speed, quality, and cost efficiency.
  • Identify systemic issues and implement best practices across studies and portfolios.
  • Manage cross-functional collaboration to support milestone achievement and issue resolution.

Conocimientos

Project management
Leadership
Communication
Client management
English proficiency

Educación

Bachelor’s Degree Life sciences

Herramientas

MS Office
PowerPoint
Excel

Descripción del empleo

IQVIA is seeking a Clinical Project Management Director in Madrid to lead a team responsible for the clinical delivery of complex, multi-regional studies and programs. You will drive strategic decision-making, ensure on-time, high-quality delivery, and manage financial performance and customer satisfaction.

The role requires seasoned leadership with strong communication and collaboration skills, and a deep understanding of clinical trial conduct and regulatory requirements.

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