Clinical trial coordinator supporting project teams across assigned studies in a fast-paced research environment. Responsibilities include coordinating trial activities, managing documentation systems, performing regulatory compliance reviews, and providing administrative support to cross-functional teams.
Responsibilities
Coordinate and oversee assigned trial activities according to specific role requirements and task matrices
Conduct department, internal, country, and investigator file reviews; document findings in appropriate systems
Maintain study-specific documentation, electronic TMF systems, and project-level tracking tools
Process regulatory documents, transmit to client and IRB/IEC, and track local compliance documentation
Analyze study metrics, reconcile findings reports,



and assist with site documentation clarifications
Requirements
High school diploma or equivalent; bachelor's degree preferred
At least 4 years of relevant clinical operations or trial coordination experience
Proficiency in MS Office and clinical trial database systems
Strong knowledge of ICH GCP guidelines and country-specific regulations
Excellent English language skills and local language proficiency as needed
Ability to successfully complete PPD clinical training program
Strong organizational skills, attention to detail, and ability to manage multiple tasks

📌 Fsp Clinical Trial Coordinator Ii (Xico)
🏢 Thermo Fisher Scientific
📍 Xico