FSP Clinical Trial coordinador II

Coordinate and oversee functions on assigned trial activities. Ensure tasks are performed on time and within budget while communicating risks to project leads. Support maintenance of study documentation and provide system support for tools like GoBalto and eTMF. Assist with scheduling client meetings and review local regulatory documents.

High school diploma or equivalent required; Bachelor's degree preferred. At least 4 years of relevant experience in clinical trials. Strong organizational skills and ability to analyze project-specific data. Proficiency in MS Office and clinical trial database systems.