Overview In this Centralized Monitoring Analyst role within IQVIA’s Cluepoints team, you will set up, program, and refresh the CM platform according to the CMP. You’ll support the Centralized Monitoring Lead by shaping study-specific CM elements
Overview In this role you shape and govern the Statistical Computing Environment to enable efficient evidence generation, regulatory readiness, and modern analytics across clinical development. You will partner with Biometrics, Data Science, IT, Quality, and external
Overview As SDTM & CRF Design Lead you will oversee end-to-end SDTM activities on a sponsor-dedicated project. You will manage CRF design from the protocol, validate vendor specifications, and define SDTM specifications across studies. You’ll collaborate
Overview In this role you enable clinical programming teams to operate in UCB’s modern Statistical Computing Environment, translating reporting needs into governed study setups and compliant platform operations. You will partner with cross-functional teams to improve how
OverviewThe Associate Director, Biostatistics is responsible for statistical activities in support of clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical