Statistical Science Director – Late Oncology and Hematology Overview • The Statistical Science Director leads biometrics teams in oncology and hematology research, ensuring robust statistical design and interpretation. • Drive statistical strategies for product development, regulatory submissions, and health technology assessments. • Collaborate with cross-functional teams to quantify product benefits, risks, and uncertainties effectively. • Provide leadership in statistical methodology, promoting innovative approaches and maintaining technical excellence. • Represent the organization in external engagements, including health authorities and scientific conferences. • Mentor and develop statisticians, fostering technical growth and expertise within the team. • Ensure compliance with safety, health, and environmental strategies in statistical practices. • Lead statistical content creation for study designs, documents, and regulatory submissions. • Partner with external vendors to ensure timely and quality delivery of statistical projects. Statistical Science Director – Late Oncology and Hematology Key Responsibilities & Duties • Manage and develop a team of statisticians, ensuring effective project delivery. • Lead statistical strategies for clinical trials, regulatory submissions, and commercial activities. • Ensure the quality and accuracy of statistical designs and interpretations. • Collaborate with cross-functional teams to align statistical strategies with organizational goals. • Represent statistical expertise in internal and external decision-making forums. • Promote and implement novel statistical methodologies in relevant research areas. • Mentor junior statisticians, fostering professional growth and technical proficiency. • Ensure compliance with organizational safety, health, and environmental standards. • Collaborate with external partners to deliver high-quality statistical analyses. Statistical Science Director – Late Oncology and Hematology Job Requirements • PhD in Statistics, Mathematics, or equivalent with substantial statistical components. • Minimum of 5 years of experience in pharmaceutical development and clinical trials. • Proven track record of leading statistical teams and projects independently. • Strong technical skills in statistical methodologies and applications. • Experience in regulatory submissions and health technology assessments. • Excellent collaboration and communication skills across cross-functional teams. • Ability to mentor and develop junior statisticians effectively. • Knowledge of safety, health, and environmental compliance in statistical practices. • Familiarity with partnering with external vendors for project delivery.