Position Purpose
The Senior Programmer is responsible for all programming aspects (including analysis datasets, pooled datasets, listings, figures, and tables) of individual Phase I-IV clinical trials and project level activities for small drug project/indications (or equivalent) and supporting operational excellence by working together with the statistical scientist and biometrician.
Major Accountability:
1. Responsible for the integrity of the programming/computing solutions for multiple clinical trials (or equivalent).
2. Is the scientific lead for programming expertise liaising with Biometrician and statistical scientific counterparts within the team, across multiple clinical trials
3. Leads the full execution of final production output generation (tables, listings and graphics) for clinical trials. May lead programming activities for a relatively small project or an indication with guidance.
4. In conjunction with the Biometrician/Statistical Scientist, develop study-level programming standards and ensure compliance with project-level/company standards. With guidance, may provide support to development of project-level programming standards, following internal guidelines.
5. Ensure high quality for all deliverable and follow the processes.
6. Ensure that documents and specifications are consistent and comply with company standards by providing input into eCRF and data structures, tables, listings and figures for Phase I-IV clinical trials and submission activities.
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