Global Quality Management Lead

IQVIA Inc; Barcelona; Sur place; EUR 70 000 - 90 000; Plein temps

Résumé du poste

IQVIA is seeking a CQM Lead to drive risk-based quality initiatives across assigned business units. The role focuses on implementing quality controls, supporting risk assessment, and guiding corrective actions while ensuring compliance with GCP and regulatory expectations.

The individual will collaborate with multiple stakeholders, manage quality teams, and travel within the region as needed. A strong background in clinical trial processes and leadership is required.

Qualifications

• Expert knowledge of and experience in (minimum of 12 years) processes related to clinical trial design, planning, start up, conduct, analysis, and reporting clinical development.
• Strong knowledge of ICH, GCP, SOPs, regulatory requirements and quality management processes.
• Excellent organizational, interpersonal and communication skills.
• Demonstrated leadership and line management skills.

Responsabilités

• Leads risk-based quality initiatives and drives standardization of processes and tools.
• Develops and implements Quality Management Plans with risk assessment and mitigation actions.
• Supports quality assurance during audits and regulatory inspections as required.
• Provides guidance on GCP compliance and quality issues within the assigned business line.
• Manages staff, performance, and professional development, in line with HR policies.

Connaissances

Quality management

GCP knowledge

Regulatory knowledge

Leadership

Communication

English fluency

Travel flexibility

Formation

Bachelor/Master in Medical or Life Science

PhD preferred

Description du poste

IQVIA is seeking a CQM Lead to drive risk-based quality initiatives across assigned business units. The role focuses on implementing quality controls, supporting risk assessment, and guiding corrective actions while ensuring compliance with GCP and regulatory expectations.

The individual will collaborate with multiple stakeholders, manage quality teams, and travel within the region as needed. A strong background in clinical trial processes and leadership is required.