- Effectively design and code SAS programs for assigned projects, consistently meeting project objectives.
- Code complex SAS programs for applications designed to analyze and report clinical trial data and for electronic submissions of data in CDISC format with minimal instruction or input from the supervisor.
- Create specifications for derived/analysis datasets.
- Program analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS.
- Generate SDTM domains and ADaM datasets.
Quality Control:
- Perform quality control checks of advanced SAS code for datasets and output produced by other statistical programmers.
- Perform reviews on define.xml and create reviewers guide for SDTM and ADaM datasets.
- Review and maintain study documents per the standard process.
Other Duties:
- Perform other duties as assigned.
Technical and Communication Skills:
- Demonstrates advanced experience with all SAS language, procedures, and options commonly used in clinical trial reporting, including the Macro language, BASE SAS, SAS/STAT, and SAS/GRAPH.
- Demonstrates intermediate knowledge of electronic submissions and CDISC.
- Proven technical proficiency in supporting daily operations and ensuring that project tasks are completed accurately and on schedule.
- Effective communicator (written and verbal), especially within their area(s) of expertise.
Preferred Education and Experience:
- MS in biostatistics or a related field, with 5-8 years of experience in the pharmaceutical industry, OR
- BS in biostatistics or a related field, with 7-10 years of experience in the pharmaceutical industry.
