💼 About This Role

You'll support global QA systems in a regulated clinical research environment. Your work will ensure compliance through audits, inspections, and vendor oversight. This role combines operational QA with strategic input on policy development.

🎯 What You'll Do

• Support planning, execution, and evaluation of global QA activities
• Conduct internal audits, site inspections, and vendor assessments
• Develop and maintain Quality System documentation
• Lead or support regulatory inspections and sponsor audits

📋 Requirements

• Undergraduate degree with 4–6 years experience or college diploma with 7–9 years
• ICH-GCP guidelines and global regulatory frameworks knowledge
• Experience in audits, inspections, and vendor qualification
• Strong analytical thinking and attention to detail

✨ Nice to Have

• Background in Life Sciences, Clinical Research, or Information Technology
• Familiarity with global privacy regulations
• Experience mentoring junior staff

🎁 Benefits & Perks

• 💰 Competitive compensation
• 🏠 Flexible work arrangements including hybrid/remote
• 🩺 Comprehensive health and wellness coverage
• 📚 Professional development opportunities
• 🌍 Exposure to global clinical research projects

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Technical/QA Interview· 60 min