Drive clinical quality management through GCP compliance, risk assessment, and quality control for assigned delivery units, sponsors, or business lines. Work with global or regional teams. As an individual contributor, you will adopt and implement global Quality Management Plans within an assigned scope. The work covers clinical trial processes, regulatory requirements, SOPs, and KPIs. You will support quality improvement across project delivery and collaborate with business stakeholders.
Key Responsibilities
Plan and execute assigned Quality Management activities
Identify and assess risks through data review and quality control
Support corrective and preventive action planning
Advise teams on Positive Clinical Practice compliance
Prepare periodic quality and risk assessment reports
Requirements:
Minimum eight years in clinical development processes
Knowledge of clinical trial design, conduct, analysis, and reporting
Knowledge of national and international regulations
Knowledge of CRO or pharmaceutical industry operations
Fluent English and excellent problem-solving skills Bring clinical development expertise, GCP knowledge, and risk management capability to quality oversight at IQVIA.