Idorsia Pharmaceuticals Ltd is seeking a Senior Clinical QA Manager to enhance their QA Compliance & Auditing Team in Basel, Switzerland. The role focuses on ensuring compliance with clinical trial quality standards and regulatory expectations while collaborating with internal teams and CROs
Job Summary
The Senior CQA Manager will provide expert support for clinical trial quality ensuring compliance with ICH-GCP and global regulatory expectations.
You will be responsible for quality oversight, process improvements, inspections, audits, and training across all phases of clinical development.
The role involves leading the preparation, coordination, and follow-up activities related to health authority inspections while collaborating closely with internal teams and CROs.
Matching Summary
Match Score: 85
Idorsia Pharmaceuticals Ltd is seeking a Senior Clinical QA Manager to enhance their QA Compliance & Auditing Team in Basel, Switzerland. The role focuses on ensuring compliance with clinical trial quality standards and regulatory expectations while collaborating with internal teams and CROs.
Skills & Requirements
Must-have
Strong background in Good Clinical Practices
Minimum 6 years industry experience
≥4 years in GCP Quality Assurance
Experience with clinical electronic systems
Lead health authority inspections
Nice-to-have
Excellent negotiation and influencing capabilities
Ability to work independently in matrixed environment
Fluent in English language
Experience in international cross-cultural environments
Key Requirements
Master's degree in Pharmacy or scientific field
Minimum 6 years industry or health authority experience