Thermo Fisher Scientific seeks a Senior Clinical Trial Coordinator to support clinical operations across multiple trials in Madrid. The role involves coordinating trial activities, maintaining study documentation, managing regulatory compliance, and providing administrative and technical support to project teams.
Responsibilities
- Coordinate and oversee trial activities on assigned studies per task matrix
- Perform department, internal, country, and investigator file reviews; document findings
- Maintain study documentation, electronic TMF, and project tracking systems
- Process regulatory documents, coordinate with sites and IRB/IEC bodies
- Support RBM activities, analyze study metrics, and reconcile findings reports
Requirements
- High school diploma or equivalent; Bachelor's degree preferred
- At least 4 years of relevant clinical trial or life science 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 organizational skills, attention to detail, and ability to manage multiple tasks
- Ability to complete PPD clinical training program