Clinical Trial Associate

Job Summary

A company is looking for a Clinical Trial Associate to provide administrative and project support for clinical research studies.

Key Responsibilities

• Support TMF-related activities, including document tracking, quality control, and audits
• Assist with study start-up, maintenance, and close-out activities in collaboration with CROs and internal teams
• Coordinate meetings, generate meeting minutes, and maintain study trackers for data review and compliance

Required Qualifications

• Minimum of Bachelor's degree in Life Sciences, Health Sciences, Nursing, Public Health, or a related field
• 2+ years of experience in Clinical Operations, Clinical Research, or a related clinical trial support role
• Working knowledge of clinical trial documentation and TMF requirements
• Experience supporting TMF activities and familiarity with eTMF systems
• Proficiency in Microsoft Office and ability to build and maintain study trackers