Plan, manage and execute programming activities across multiple studies, asset(s), indications or function to deliver all data analysis outputs to agreed timelines and quality, (e.g., macros, analysis datasets, pooled datasets, tables, figures and listings for regulatory submissions and publications).
Oversee outsourced tasks to third party vendors and ensure their performance meets the agreed timelines, quality and budget requirements established for the project or study.
Define, develop and embed data standards within a function, or therapeutic area in accordance with industry standards
Responsible for programming and QC across a study/asset including submission activities adhering to relevant SOPs policies.
Participate in the design of other study delivery components (e.g. case report forms, study databases).
Review and input into key documents at the project level (e.g. submission documents, clinical report and publication). May author or co-author reporting analysis plans and department level documents (e.g. SOPs, working practice document).