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The Oncology Quality Risk Management Lead is responsible for overseeing risk management practices within clinical trials, focusing on quality and regulatory compliance. They will drive risk identification, collaborate with functional teams, and implement risk management frameworks to improve patient safety and trial reliability. The role includes managing risk strategies, maintaining governance structures, and fostering communication about risks with stakeholders.

The Late-Stage Clinical Scientist will oversee scientific integrity and data quality in oncology clinical trials. Responsibilities include authorship of trial documents, data review, safety profile analysis, and collaboration with clinical teams. The role involves maintaining clinical knowledge and participating in Health Authority meetings.

The Associate Director of Biostatistics will design, analyze, and interpret clinical trials and observational studies, providing statistical expertise for clinical development, regulatory submissions, and maximizing value from data. Responsibilities include ensuring compliance with regulatory requirements, delivering statistical analyses, and collaborating with various teams to maintain high-quality statistical output.