Obsidian Therapeutics is seeking an Associate Director, Clinical Quality to support the advancement of clinical trials in metastatic melanoma and non-small cell lung cancer. The successful candidate will be responsible for developing and executing a GCP Clinical Quality Assurance program to ensure compliance with applicable regulations.
Requirements
- Define and implement a risk-based GCP quality management system
- Develop an audit program and conduct internal and external GCP audits
- Manage the audit lifecycle activities
- Present audit findings and escalate serious non-compliance issues
- Work directly with auditees to ensure completion of corrective and preventative actions
- Identify non-compliance trends, gaps, and implement mitigation strategies
- Review study documents to assess GCP compliance
- Support investigation and closure of GCP related deviations/quality events/CAPAs
- Collaborate with Clinical Operations, Technical Operations teams and CRO counterparts
- Support Quality Management in inspection readiness activities
Benefits
- Comprehensive medical, dental, and vision coverage
- Company contributions to health savings and retirement accounts
- Ample paid time off
- Access to wellness programs
- Rich career growth opportunities