Thermo Fisher Scientific seeks a Clinical Trial Coordinator to support administrative and technical functions across assigned clinical trials. The role involves file management, site activation coordination, regulatory compliance support, and cross-functional collaboration within a general clinical research organization.
Responsibilities
Coordinate and oversee assigned trial activities and site activation functions
Perform file reviews and maintain electronic Trial Master Files (eTMF) and Investigator Site Files
Manage administrative tasks including document processing, mass mailings, and report distribution
Support site selection, feasibility activities, and investigator communications
Analyze study metrics, reconcile findings, and assist with regulatory compliance packages
Requirements
High school diploma or equivalent; Bachelor's degree preferred
0–1 year experience in clinical research or related field
Proficiency with clinical trial management systems (Activate, eTMF)
Knowledge of clinical trial SOPs and regulatory guidelines
Strong organizational and documentation skills
Ability to manage multiple tasks and meet deadlines

📌 Fsp Ctc I (Xico)
🏢 Thermo Fisher Scientific
📍 Xico