SAS/Statistical Programmer
Green Key Resources
United States
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Summary
The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry. The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting. The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.
Responsibilities
The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry. The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting. The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.
Responsibilities
- Develop and validate SAS programs to support clinical trial data analysis and reporting
- Create, maintain, and document SAS programming standards and procedures
- Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to ensure programming requirements are met
- Perform data checks, quality control checks, and data review activities to ensure data accuracy and consistency
- Prepare datasets for analysis, including merging and cleaning data from various sources
- Prepare and review tables, listings, and figures for clinical study reports
- Ensure compliance with regulatory requirements and guidelines
- Keep up-to-date with new SAS programming methods and software, as well as regulatory guidance.
- Bachelor's Degree in statistics, computer science, or a similar quantitative field
- 5 years of clinical statistical programming experience within the pharmaceutical or related industry
- Proficiency in SAS programming
- Knowledge of CDISC data standards
- Strong attention to detail and ability to work independently
- Excellent problem-solving skills
- Excellent verbal and written communication skills
- Ability to work in a team environment and collaborate effectively with other stakeholders
- Knowledge of regulatory requirements for clinical trials and drug development.
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Seniority level
Mid-Senior level -
Employment type
Full-time -
Job function
Research, Analyst, and Information Technology -
Industries
Staffing and Recruiting
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