The role involves performing statistical programming activities and leading one or more studies within the Project Based Services team. Responsibilities include providing scientific leadership, ensuring compliance and quality, and managing people development.
Develop R and R Shiny dashboards and applications to support clinical trial data review and decision-making. Create reusable code and visualizations to transform complex data into actionable insights.
The candidate will program and validate complex datasets, SDTMs, and non-efficacy outputs for oncology studies. They will also lead programming teams, develop standard macro libraries, and ensure compliance with SOPs and regulatory requirements.
The role involves providing statistical expertise and scientific leadership for pharmaceutical studies in areas such as oncology, GI, neuroscience, or infectious diseases. Responsibilities include managing compliance, quality, governance, and people development.
Lead late-phase studies by providing expert statistical guidance and developing essential documentation such as SAPs and protocols. Oversee the creation of complex dataset specifications and ensure quality control of clinical trial outputs.
The role involves providing statistical expertise and scientific leadership for pharmaceutical clients, primarily focusing on neuroscience studies. Responsibilities include managing compliance, quality, governance, and people development.
Lead and deliver SDTM mapping and conversion activities for Real-World Data to CDISC standards. Act as a Subject Matter Expert to develop ECRT packages and collaborate cross-functionally to ensure quality delivery.
The role focuses on providing statistical expertise and scientific leadership for a key pharmaceutical client within the FSP function. Responsibilities include overseeing technical analysis, people development, and ensuring compliance and quality governance.
The role involves providing statistical expertise and scientific leadership for oncology studies within a pharmaceutical client's FSP function. Responsibilities include managing compliance, quality, governance, and people development.
Lead studies and manage sponsor systems by programming and validating complex datasets and SDTMs. Act as a lead programmer across multiple studies, ensuring quality delivery and coordinating with statisticians and project managers.
Provide statistical expertise and scientific leadership for global pharmaceutical clients focusing on GI, oncology, neuroscience, or infectious disease studies. Responsibilities include authoring SAP/TLF shells and validating ADaM/TLFs for DMC, IA, and CSR.
The role involves programming and validating complex efficacy datasets, summary tables, and figures for clinical trials. It also requires producing and reviewing Statistical Analysis Plans (SAPs) and other critical study documentation.
The role involves providing statistical expertise and scientific leadership for pharmaceutical studies in oncology, GI, neuroscience, or infectious diseases. Responsibilities include managing compliance, quality, governance, and leading people development within the FSP team.
Provide statistical expertise and scientific leadership for GI and Oncology studies within a pharmaceutical client setting. Responsibilities include authoring SAP/TLF shells and validating ADaM/TLFs for DMC, IA, and CSR.
