Lead clinical quality planning and GCP compliance for IQVIA assignments across global delivery teams. This is a full time individual contributor role.
As a Clinical Quality Manager, you will implement quality plans, assess risk, and support corrective actions across assigned business lines. The position requires clinical development expertise, regulatory knowledge, and familiarity with CRO or pharmaceutical operations. You will work with Quality Management, Quality Assurance, functional teams, and other stakeholders to maintain quality in project delivery.
Key Responsibilities: Implement global Quality Management Plans within assigned scopes
Identify and assess risks through data review and quality control
Advise teams on Positive Clinical Practice compliance
Manage non-compliance and support corrective actions
Prepare periodic quality and risk assessment reports
Requirements: Minimum eight years in clinical development processes
Knowledge of national and international regulations
Understanding of drug development processes
Clinical Research Organization or pharmaceutical operations knowledge
Fluent English and excellent problem solving skills
Apply clinical development expertise, risk assessment, and GCP knowledge to quality management work at IQVIA.