Clinical Trial Documentation Coordinator

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.