- To provide SAS programming support for the Clinical Research Programming Department
- Develop and document programs to create analysis datasets summarizing key clinical trial data
- Develop and document programs and to produce tables, listings and other reports and analyses summarizing clinical trial results
- Perform and document quality control checks for programs
- Assist in testing and implementation of new and updated internally and externally developed software as well as new SAS releases
- Participate in the development and review of study-specific procedures; participate in clinical project team meetings as required
- Assist with the development of case report forms
- This is not an exhaustive, comprehensive listing of job functions
- May perform other duties as assigned
- Contacts Inside the Company
- Clinical Research Programming
- Education: Bachelor’s degree or equivalent in computer science, mathematics or other scientific field (or equivalent theoretical/technical depth)
- Minimum of 5 years of experience programming and analyzing scientific data in a pharmaceutical / clinical trial environment
- Expertise in SAS programming language
- Experience working in a PC SAS environment
- Must have good organization and written and oral communication skills
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