Associate Director, Quality Risk Specialist
KI-Beschreibung
In this role, you will focus on developing and implementing risk-based quality management strategies for clinical trials. Your day-to-day responsibilities will involve collaborating with various teams to ensure compliance, address quality issues, and enhance processes throughout the study lifecycle.
Anforderungen
8 Jahre- •Minimum 8+ years QA experience or relevant experience in quality management, biomedical science, clinical development, or regulatory compliance
- •B.S. and
/ or M.S. in Chemistry, Biology, or Health or Quality related field or equivalent combination of education, training, and experience - •Demonstrated applied knowledge of ICH
/ GCP, regulatory guidelines/ directives, clinical research processes and principles of Quality Assurance