Bachelor's Degree in statistics, computer science, or related field
4+ years of clinical statistical programming experience in the pharmaceutical industry
Proficiency in SAS programming
Familiarity with CDISC data standards
Strong attention to detail
Excellent problem-solving abilities
Strong communication skills, both verbal and written
Knowledge of regulatory requirements for clinical trials
Ability to collaborate effectively in teams
Responsibilities
Ensure accuracy and consistency of clinical data
Collaborate closely with Biostatisticians and Clinical Research teams to develop programming solutions
Develop and validate SAS programs for clinical trial data analysis
Create, maintain, and document SAS programming standards
Perform data quality checks and review activities
Prepare datasets for analysis by merging and cleaning data
Prepare and review tables and listings for clinical study reports
Ensure compliance with regulatory requirements and stay updated on programming methods
Benefits
Comprehensive health, dental, and vision insurance
Retirement plans with company match
Flexible work hours and remote work options
Professional development and training opportunities
Employee wellness programs
Paid time off and holidays
Full Job Description
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
Requirements:
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
bility to work in a team environment and collaborate effectively with other stakeholders
