Research Analyst

• Monitor clinical studies across various oncology trials and ensure accurate, complete, and timely submission of study data and documents
• Prepare high-quality monitoring visit reports and follow-up letters in a timely manner
• Confident use of relevant study systems, e.g., WBDC, IVRS, ... and maintenance of the CTMS
• Participate in international study team meetings and investigator meetings
• Contribute to site selection and assess recruitment potential
• Initiate study sites, provide training, support, and guidance to site staff
• Continuously monitor recruitment performance, site performance, and data quality; escalate issues to study management
• Proactively communicate with the study site and the local study team

Clinical Research Associate, CRA

Senior Clinical Research Associate – Sponsor Dedicated

Research Analyst – German Speaking

Clinical Research Associate – Senior

Data Research Analyst – Loans