Clinical Trial Documentation Coordinator

IQVIA

Full-time Sector sanitario
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Location
Mexico, ciudad de mΓ©xico, Mexico
Posted
July 13, 2026

Job Description

IQVIA Mexico City is seeking a Clinical Trial Administrative Assistant to support the Clinical Research Associates and Regulatory and Start-Up teams in delivering a complete Trial Master File. You will help maintain documents, prepare reports, and ensure alignment with project timelines.

Ideal candidates have a life sciences or health degree and at least one year in clinical research, with fluent English and strong communication skills. Proficiency in Word, Excel, and PowerPoint is essential.

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