Research Analyst

• Deliver clinical trial monitoring work to a high standard
• Coordinate all activities for setting up and monitoring a study
• Complete accurate study status reports and maintain study documentation
• Run sponsor generated queries efficiently and take responsibility for study cost efficiency
• Participate in the preparation and review of study documentation and feasibility studies for new proposals as required
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
• Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements

Clinical Research Associate

• Levantamiento de información de estudios asignados desde su aprobación inicial hasta la presentación de resultados
• Estructurar cuestionarios y presentaciones

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Clinical Research Associate

Research Analyst – L7