Clinical Trial Coordinator- FSP (client dedicated) - Belgium or Netherlands

Thermo Fisher Scientific seeks a Clinical Trial Coordinator to support a dedicated client team across Belgium and Netherlands. The role involves coordinating trial activities, managing documentation systems, and providing administrative support to global clinical operations.

Responsibilities

• Coordinate and oversee assigned clinical trial activities according to task matrices and study requirements
• Perform file reviews for departments, internal teams, countries, and investigators; document findings in appropriate systems
• Maintain study-specific documentation and electronic Trial Master Files with regular reviews and updates
• Provide system support for GoBalto, eTMF, and other clinical trial platforms
• Process documents for client submission, organize meetings, and distribute investigator site files and materials to trial sites

Requirements

• High school diploma or equivalent; bachelor's degree preferred
• At least 4 years of relevant experience in clinical operations or equivalent combination of education and training
• Fluent in Dutch and English; French language skills ideal
• Strong proficiency with MS Office and ability to master clinical trial database systems
• Knowledge of ICH Good Clinical Practices and country-specific regulations
• Excellent organizational skills with demonstrated ability to manage multiple concurrent tasks
• Ability to successfully complete PPD clinical training program