Senior SAS Statistical Programmer for Clinical Trials Data

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

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.