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 Valuable 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.

📌 Clinical Quality Manager GCP Compliance (Kirkland)
🏢 IQVIA
📍 Kirkland