Associate Director, Quality & Risk Management

IQVIA; Madrid; On-site; EUR 90,000 - 130,000; Full time

Job summary

IQVIA in Madrid is seeking a CQM Lead to drive quality management initiatives across clinical programmes. The role focuses on implementing risk-based quality controls and providing strategic guidance on GCP compliance.

Requires a minimum of 12 years in clinical trial processes, advanced degrees, and fluent English. Travel within the region may be required. Leadership responsibilities include directing teams and collaborating with cross-functional stakeholders.

Qualifications

• Minimum 12 years in processes related to clinical trial design, planning, start up, conduct, analysis, and reporting.
• Knowledge of ICH, GCP, SOPs and regulatory requirements.
• Excellent organizational, interpersonal and communication skills.

Responsibilities

• Leads quality management initiatives and risk-based approaches across assigned units.
• Advises stakeholders on quality control, risk assessment, and corrective/preventive actions.
• Plans and implements Quality Management activities and reports.
• Supports audits and regulatory inspections as required.

Education

Bachelor's or Master's in Medical/Life Science

PhD preferred

Tools

Microsoft Office

Job description

IQVIA in Madrid is seeking a CQM Lead to drive quality management initiatives across clinical programmes. The role focuses on implementing risk-based quality controls and providing strategic guidance on GCP compliance.

Requires a minimum of 12 years in clinical trial processes, advanced degrees, and fluent English. Travel within the region may be required. Leadership responsibilities include directing teams and collaborating with cross-functional stakeholders.