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.
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.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Staffing and Recruiting
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