Job Description

• Performs programming tasks as assigned by study project team leads that

includes but is not limited to independently creating, executing, maintaining, and
validating programs that transfer data across multiple data management systems
or operating systems, combining data from a variety of sources and structures,

reports or combining multiple databases and validating programs that generate
listings, tables and figures using SAS and standard tools and processes.

• Prepares and analyzes clinical trial patient datasets, such as laboratory data, vital

signs data, tumor response data, imaging data, quality of life and well-being
questionnaire data, or adverse events data, for clinical research purposes.
Consult with researchers and multi-disciplinary project teams to analyze
problems and recommend technology-based solutions and computational
strategies for the specific project as assigned.

• Develops the customized codes to utilize existing tools and applications to

provide the outputs or to validate outputs for clinical bioinformatics or technical
use.

• Acts as the programming lead on studies of simple to moderate complexity to

deliver on lead tasks/responsibilities.

• Actively seeks information to gain good understanding of the role of the lead

programmer in the overall process and may act as the lead programmer on
simple to moderately complex projects under close supervision. Ensures
adherence to departmental working practice documents and SOPs, and
contributes to the development informal training materials.

• Increases knowledge base and professional skills in areas including

programming, technology and techniques, clinical trials, and the pharmaceutical
industry by working closely with mentors, attending presentation / teaching
events, and contributing to other general department documents and policies by
assisting mentors with implementing best practice documents and articles.