Associate Director, Quality Management — Clinical Trials

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

Descripción de la vacante

IQVIA is seeking a CQM Lead to drive risk-based quality management across designated study units and to implement quality improvement initiatives. You will advise stakeholders on quality control, risk assessment, and corrective actions, ensuring alignment with GCP and ICH guidelines across clinical development.

The role requires a 12+ year track record in clinical trials, strong leadership, excellent communication, and the ability to travel within the region.

Formación

• Bachelor’s or Master’s degree in Medical or Life Science; PhD preferred.
• 12+ years of experience in clinical trial design, planning, start-up, conduct, analysis, and reporting.
• Strong knowledge of ICH, GCP, SOPs, regulatory requirements, and quality management processes.
• Excellent organizational, interpersonal and communication skills.
• Ability to travel within the region.
• Fluent in English.

Responsabilidades

• Leads risk-based quality and study management to strengthen standardized processes.
• Develops and implements Quality Management Plans and risk mitigation actions.
• Collaborates with business lines and stakeholders to maintain quality during project delivery.
• Provides guidance on GCP compliance and assists during audits and inspections.
• Manages staff per policies and supervises performance and development.
• Performs additional tasks as required by the Head of the relevant business line.

Conocimientos

Fluent in English

Leadership and people management

Quality management

Risk-based quality management

Clinical development knowledge

Educación

Bachelor’s or Master’s degree in Medical or Life Science

PhD preferred

Herramientas

Microsoft Office

Descripción del empleo

IQVIA is seeking a CQM Lead to drive risk-based quality management across designated study units and to implement quality improvement initiatives. You will advise stakeholders on quality control, risk assessment, and corrective actions, ensuring alignment with GCP and ICH guidelines across clinical development.

The role requires a 12+ year track record in clinical trials, strong leadership, excellent communication, and the ability to travel within the region.