
The Associate Director, Epidemiology Analytics role within the Clinical Safety and Pharmacovigilance group at Daiichi Sankyo focuses on leveraging clinical trial and real-world data to ensure drug safety. Key responsibilities include developing statistical analysis plans for signal detection, conducting complex epidemiologic research such as cohort studies and data mining, and creating automation platforms to enhance data processing. The position requires collaboration with global cross-functional teams to manage adverse event evaluations and prepare regulatory submissions. This opportunity appeals to professionals seeking to drive meaningful impact on patient health through innovative pharmaceutical research. The role offers a dynamic environment with opportunities for mentorship, strategic thinking, and occasional travel, supporting a mission to improve lives worldwide.


















