FSP Clinical Trial Coordinator

Thermo Fisher Scientific seeks a Clinical Trial Coordinator to support clinical operations across multiple trials. The role involves coordinating trial activities, maintaining documentation systems, managing regulatory compliance, and serving as a liaison between project teams and sites.

Responsibilities

• Coordinate and oversee assigned trial activities including central or local functions per task matrix
• Conduct department, internal, and investigator file reviews and document findings in systems
• Maintain study-specific documentation, global support systems, and electronic TMF records
• Process regulatory documents, manage vendor trackers, and support RBM activities
• Organize and facilitate client and internal meetings, compile investigator site files and materials

Requirements

• High school diploma or equivalent; bachelor's degree preferred
• At least 4 years of relevant experience in clinical trial operations or related field
• Strong proficiency in MS Office and clinical trial database systems
• Excellent English language skills and local language proficiency as needed
• Knowledge of ICH Good Clinical Practices and applicable country regulations
• Demonstrated organizational skills and attention to detail with multitasking ability
• Ability to complete PPD clinical training program successfully