Senior Quality Management Lead – Clinical Trials

IQVIA Inc; Reading; On-site; GBP 90,000 - 130,000; Full time

Job summary

IQVIA in Reading, United Kingdom seeks a seasoned quality management lead to drive risk-based approaches across clinical trials. You will develop and implement quality systems to improve study delivery and ensure regulatory compliance.

You will mentor teams, plan audits, track quality metrics, and collaborate with line managers to deliver compliant, high-quality outcomes. 12+ years in clinical trial processes required; fluent English.

Qualifications

• Bachelor’s or Master’s degree in Medical or Life Science required; PhD preferred.
• Expert knowledge of and experience in (minimum of 12 years) clinical trial design, planning, start up, conduct, analysis and reporting.
• Sound knowledge of ICH, GCP, SOPs, regulatory requirements and quality management processes.

Responsibilities

• Lead quality management initiatives across designated trials and units.
• Develop, implement and monitor the Quality Management Plan and risk-based approaches.
• Provide guidance on regulatory compliance and CAPA processes.
• Support audits and regulatory inspections as required by SOPs.

Skills

Leadership

Communication

Judgement

Negotiation

Problem-solving

MS Office

Team management

Education

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

PhD preferred

Tools

Microsoft Office

Job description

IQVIA in Reading, United Kingdom seeks a seasoned quality management lead to drive risk-based approaches across clinical trials. You will develop and implement quality systems to improve study delivery and ensure regulatory compliance.

You will mentor teams, plan audits, track quality metrics, and collaborate with line managers to deliver compliant, high-quality outcomes. 12+ years in clinical trial processes required; fluent English.