What are the responsibilities and job description for the Statistical Programmer position at Katalyst CRO?
Responsibilities
- The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.
- 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
- 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
- The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry
- 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
- 4 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
- Knowledge of regulatory requirements for clinical trials and drug development
- Ability to work in a team environment and collaborate effectively with other stakeholders