Statistical Programmer

Katalyst CRO; North Chicago (IL); On-site; USD 95,000 - 125,000; Full time

Job summary

Katalyst CRO is seeking an experienced SAS Programmer to support clinical data analysis and reporting in a fast-paced pharmaceutical context. The role involves developing and validating SAS programs, ensuring data accuracy, and maintaining programming standards.

The candidate will collaborate with Biostatisticians, Data Managers, and Clinical Research teams to ensure regulatory compliance and timely deliverables.

Qualifications

• Bachelor's degree in statistics, computer science, or a similar quantitative field.
• 4+ years of clinical statistical programming experience.
• Proficiency in SAS programming.
• Knowledge of CDISC data standards.
• Knowledge of regulatory requirements for clinical trials.
• Strong problem-solving and communication skills.

Responsibilities

• Ensure accuracy and consistency of clinical data.
• Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to develop programming solutions.
• Develop and validate SAS programs to support data analysis and reporting.
• Create, maintain, and document SAS programming standards and procedures.
• Prepare datasets for analysis by merging and cleaning data from various sources.
• Prepare and review tables, listings, and figures for study reports.
• Ensure compliance with regulatory requirements and guidelines.
• Keep up to date with SAS programming methods and regulatory guidance.

Skills

Attention to detail

Independent work

Communication skills

Team collaboration

Problem solving

Regulatory knowledge

Education

Bachelor's Degree in statistics, computer science, or a similar quantitative field

Tools

SAS

CDISC

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
• Ability to work in a team environment and collaborate effectively with other stakeholders