What are the responsibilities and job description for the Statistical Programmer position at Katalyst CRO?
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.
- 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.
