Senior Clinical SAS Programmer
4 weeks ago
Job Summary
The Senior Clinical SAS Programmer will design, develop, evaluate, and modify computer programs to analyze and evaluate clinical data. This role requires a strong understanding of programming languages, including SAS Macros, SQL, STATS, graph, and ODS, as well as knowledge of databases and CDISC SDTM and ADaM models and data mapping process.
Key Responsibilities
- Collaborate with statisticians and other functions to plan clinical programming deliverables, including data cleaning, extraction, and integration programs, web reporting programs, integrity reports, analysis datasets, CDISC SDTM and ADaM data mappings, CSR tables, listings, and figures.
- Develop and review programming specifications for various types of deliverables by applying SAS programming.
- Contribute to the development of Data Management and Validation Plan, Statistical Analysis Plan, Table shells, and other related documents within the capacity of clinical programming.
- Perform all other project and process-related activities assigned by the supervisor, such as documentation of deliverables, timelines, client communication, etc.
- Contribute to on-going data quality improvement efforts within assigned projects using SAS and other proprietary software.
Requirements
- Master's Degree/Bachelor's Degree in Mathematics, Statistics, Engineering, Computer Science/Applications, Pharmacy, or any other similar type of qualification.
- At least six years (Lead)/Four years (Senior) of Clinical SAS programmer experience in Pharmaceutical/CRO.
- Good knowledge of programming languages (SAS Macros, SQL, STATS, graph, and ODS) with an understanding of databases.
- Knowledge of CDISC SDTM and ADaM models and data mapping process is desirable.
- Good analytical skills with the ability to process scientific and medical data.
- Knowledge of regulatory submission process.
- Knowledge in development, documentation, and testing of analysis data and programming code to meet regulatory and company standards.
- Understanding of GCP principles and other regulatory standards in Clinical Research.
- Good organizational and communication (written and oral) skills, ability to manage multiple tasks, ability to work with minimum supervision, as well as in a team environment and a desire to improve skills.
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