Exciting opportunity for a hybrid SAS/Statistical Programmer to work in the oncology field! Join a dynamic team and contribute to meaningful work providing programming support for clinical trials conducted within the pharmaceutical industry.
Job Detail
Job Description
Key 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
Qualifications:
- 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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