Clinical Research

• 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
• Take responsibility for study cost efficiency
• Participate in preparation and review of study documentation and feasibility studies for new proposals
• Develop and maintain collaborative relationships with key stakeholders, clinical investigators, and site staff
• Ensure patient safety and compliance with ICON's procedures, protocols, and regulatory requirements

Explore CRA I, CRA II, Senior CRA at ICON plc. Review requirements and application details.

Clinical Research jobs in Japan

CRA I, CRA II, Senior CRA

Clinical Trial Manager