A company is looking for a Clinical Program Quality Manager.
Key Responsibilities
Support GCP compliance activities for oncology clinical trials through audit and compliance strategies
Conduct audits of investigator sites and internal systems to ensure adherence to GCP and regulatory requirements
Manage quality investigations and provide support during regulatory inspections
Required Qualifications
Bachelor's degree in Pharmacy, Regulatory Affairs, Clinical or related field
5 years of related experience in clinical quality management
Knowledge of GCP and GVP regulations and ICH Guidelines
Experience in identifying and investigating quality issues
Ability to manage and track team projects and timelines
Quality Manager • Tempe, Arizona, United States