💼 About This Role

You'll lead quality assurance audits for global clinical trials, ensuring compliance with regulatory standards. You'll drive root cause analysis and corrective action plans to resolve quality events. This role offers remote flexibility in a science-driven environment impacting patient safety.

🎯 What You'll Do

• Lead and execute comprehensive quality audits of clinical trial processes.
• Manage quality event case handling through full lifecycle resolution.
• Conduct root cause analysis and develop corrective and preventive actions.
• Monitor quality metrics and escalate critical issues to senior management.

📋 Requirements

• Bachelor's degree in a scientific, healthcare, or related field
• 6–7+ years in quality assurance, compliance, or clinical research
• Experience in GCP, GxP, and regulatory frameworks in pharma or clinical trials
• Proven experience in quality audits, regulatory inspections, or quality event management

✨ Nice to Have

• MBA or Master's degree
• Lean Six Sigma certification
• Experience with continuous improvement methodologies

🎁 Benefits & Perks

• 💵 Competitive compensation aligned with experience
• 🏠 Remote work flexibility with global collaboration
• 🏥 Comprehensive health insurance for employees and families
• 💰 Retirement and financial planning support
• 🌍 Employee assistance program with 24/7 well-being support

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter screening· 30 min
2. 2Hiring manager interview· 45 min
3. 3Technical/audit assessment· 60 min