Clinical Quality Manager GCP Compliance
18 hours ago
Kirkland, Montreal (administrative region), Canada
IQVIA
Full-time
€90,000 - €130,000/year
Free with email or Google
Save this job and keep your search organized
Create a free account to save jobs, create alerts and return to this listing from your dashboard.
Free with email or Google
By continuing, you agree to our Terms & Privacy Policy.
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 Good 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.
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 Good 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.