Research Analyst

• Monitoring of clinical trials across various oncology therapy areas, including ensuring correct, complete and timely submission of study data and documents, and active participation in all study phases (feasibility, set-up, recruitment, maintenance, DBL, closure)
• Timely preparation of high-quality reports and follow-up letters for monitoring visits
• Confident use of relevant study systems, e.g., WBDC, IVRS, etc., and maintenance of the CTMS
• Participation in international study team meetings and investigator meetings
• Support in the selection of investigational sites and assessment of recruitment potential
• Site initiation, training, support and guidance of site personnel
• Continuous monitoring of recruitment performance, site performance and quality, and escalation of deficiencies to study management
• Proactive communication with study sites and the local study team

Clinical Research Associate – Oncology

Clinical Research Associate (CRA) – Oncology