Champion the development of bioanalytical assays and strategies for multiple oncology programs. Collaborate with external vendors and internal teams to ensure compliance and drive innovative solutions in clinical-stage bioanalysis.

Drive the development of high-quality SAS programming deliverables, ensuring compliance with CDISC and regulatory standards. Provide technical leadership and collaborate cross-functionally to enhance statistical programming practices and efficiency.

Champion quality assurance excellence in clinical development, fostering collaboration across functions to enhance compliance, inspection readiness, and continuous improvement. Drive innovative approaches that strengthen organizational capabilities and ensure regulatory alignment.

Champion high-quality SAS programming for clinical trials, ensuring compliance with CDISC and regulatory standards. Lead programming activities, collaborate cross-functionally, and enhance statistical programming processes within the Biometrics department.

Develop and execute innovative clinical pharmacology strategies for oncology assets, utilizing advanced pharmacometric modeling and simulation to guide decision-making and study design throughout the drug development process.