Thermo Fisher Scientific seeks a Clinical Trial Coordinator II to provide administrative and technical support to clinical trial projects. The role involves coordinating trial activities, managing documentation, maintaining regulatory compliance, and serving as a liaison across functional teams in a Buenos Aires office setting.
Responsibilities
Coordinate and oversee assigned clinical trial activities according to task matrix and study protocols
Perform regulatory file reviews and maintain electronic trial master file (eTMF) documentation
Manage administrative tasks including document processing, communications, and meeting organization
Support scheduling of client and internal meetings; provide system support for GoBalto and eTMF
Analyze study metrics, reconcile findings,



and assist with investigator site file distribution to trial sites
Requirements
High school diploma or equivalent; Bachelor's degree preferred
At least 4 years of relevant experience in clinical operations or trials
Strong organizational skills with attention to detail and multitasking ability
Proficiency in MS Office and clinical trial database systems
Knowledge of ICH Good Clinical Practices and local country regulations
Excellent English language skills and local language proficiency
Ability to complete PPD clinical training program

📌 Fsp Clinical Trial Coordinador Ii (Buenos Aires)
🏢 Thermo Fisher Scientific
📍 Buenos Aires