We are seeking an Associate Director of Clinical Quality Assurance to oversee compliance with GCP/GVP regulations and internal policies. The ideal candidate will have a strong background in FDA regulated industry and experience with Veeva Quality Docs.
Requirements
- Minimum 10 years of experience in FDA regulated industry
- Previous hands-on experience with Veeva Quality Docs, Veeva Training, and Veeva QMS
- Strong customer focus and ability to prioritize and adapt to business needs
Benefits
- Comprehensive health coverage
- Flexible time off
- Paid holidays
- Year-end shutdown
- Monthly wellness stipend
- 401(k) match
- Tuition reimbursement
- Commuter benefits
- Disability and life insurance
- Annual bonus opportunities
- Equity grants