Clinical Trial Associate III

Job Summary

To support biotech, medtech, and specialty pharma companies, the full-time Clinical Trial Associate III will assist in electronic Trial Master File administration, maintain operational tracking tools, and participate in project team meetings while working remotely on a contract basis.

Key responsibilities

• Assist in eTMF filing and administration, ensuring document completeness and conducting final site level reviews
• Create and maintain tracking tools for operational data, including Key Performance Indicators (KPIs) and quality metrics
• Participate in project team meetings, prepare meeting minutes, and maintain action/decision logs

Required qualifications

• Bachelor's degree or international equivalent in a clinical, biological, scientific, or health-related field
• 2 to 5 years of practical experience with clinical trial administration
• Strong knowledge of clinical studies and Trial Master File functionality
• Ability to work independently and manage multiple projects in a fast-paced environment