Job Description:
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- To provide SAS programming support for the Programming functional area.
- Main Focus: receive general instructions; Complete assignments accurately and in a timely fashion with no supervision; anticipate & investigate unexpected difficulties with program/data
- Develop and document programs to create/verify analysis datasets summarizing key clinical trial data
- Develop and document programs to produce/verify tables, listings and other reports and analyses summarizing clinical trial results
- Perform quality control checks for programs and data
- Review the protocol, case report forms, and Data Management documents
- Review and discuss Statistical Analysis Plan (SAP) and statistical programming specifications
- Create analysis databases and generate analyses and reporting outputs
- Demonstrate a good understanding of FDA, ICH and CDISC guidelines
- Interact with CROs and review their deliverables as needed
- Review programming deliverables from team members if needed
- This is not an exhaustive, comprehensive listing of job functions. May perform other duties as assigned
- 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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