Clinical Trial Associate

Job Summary

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

Key Responsibilities

• Coordinate and assist with trial start-up activities, including budget and contract negotiations
• Track study documentation and monitor study progress, including site activation and patient enrollment
• Lead the management of the Trial Master File (TMF) and ensure all essential study documents are organized

Required Qualifications

• Minimum Bachelor's degree in a life science-related field
• 2+ years' experience in a clinical trials research environment
• General knowledge of regulatory requirements and Good Clinical Practice (GCP)
• High proficiency in Veeva Vault CTMS and eTMF systems
• Proficient in Microsoft Office or Google Suite