Clinical Trial Coordinator II supporting pharmaceutical and biotech clinical trials across multiple countries. Coordinates trial activities, maintains study documentation, manages regulatory files, and provides administrative and technical support to project teams.
Responsibilities
Coordinate and oversee assigned clinical trial activities according to role specifications
Conduct department, internal, country, and investigator file reviews; document findings
Maintain study documentation, track training requirements, and ensure eTMF compliance
Process regulatory documents, manage vendor trackers, and transmit documents to clients and IRB/IEC
Analyze study metrics, reconcile findings reports, and provide administrative support to team members




Requirements
High school diploma or equivalent; bachelor's degree preferred
At least 4 years of relevant clinical trial or related experience
Strong knowledge of ICH Good Clinical Practices and country regulations
Proficiency in MS Office and clinical trial database systems (GoBalto, eTMF)
Excellent English language skills; local language proficiency as needed
Demonstrated ability to manage multiple tasks with attention to detail
Ability to complete PPD clinical training program

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