Clinical Trial Associate III

Job Summary

A company is looking for a Clinical Trial Associate III (Contract).

Key Responsibilities

• Assist in eTMF filing and administration, including document submission, review, and final collection
• Create and maintain tracking tools and databases for operational data, including 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
• 5+ years of practical experience in clinical trial administration (e.g., Inhouse CRA, CTA, site administration)
• Strong knowledge of clinical studies and TMF functionality in accordance with study-specific plans and SOPs
• Ability to work independently and manage multiple projects in a fast-paced environment
• Preferred location: East Coast