Senior CRA Coordinator – Site Monitoring & Trials

IQVIA LLC is seeking a Clinical Research Associate to perform site management and monitoring for various clinical protocols in Mexico City. Key responsibilities include ensuring adherence to Good Clinical Practice standards and managing site performance.

The ideal candidate will have a Bachelor's degree, at least 5 years of monitoring experience, and strong organizational skills. Proficiency in Excel and PowerPoint is also needed. Join us in improving patient outcomes through innovative medical treatments.