SAS Programmer

Venesco,-LLC-; Frederick (MD); On-site; USD 100,000 - 140,000; Full time

Job summary

Venesco, LLC seeks skilled SAS Programmers to develop validated statistical programs and CDISC-compliant datasets for clinical trials, safety reporting, and FDA submissions. You will collaborate with CDM and Biostatistics teams to ensure high-quality analyses.

Responsibilities include creating TLFs, SDTM/ADaM datasets, define.xml, validation plans, and supporting interim and final analyses through regulatory-ready programming.

Qualifications

• Bachelor's degree in Statistics, Computer Science, Mathematics, or related field.
• SAS Advanced Programmer Certification required.
• Minimum 7 years of clinical SAS programming experience.
• Extensive experience with CDISC, SDTM, and ADaM standards.
• Experience supporting FDA submissions.
• Strong knowledge of validation practices and regulatory requirements.

Responsibilities

• Develop and validate SAS programs.
• Produce Tables, Listings, and Figures (TLFs).
• Generate SDTM, ADaM, and SEND datasets.
• Develop define.xml files and reviewer guides.
• Create programming validation plans and reports.
• Develop randomization programs and statistical outputs.
• Support interim and final analyses.
• Assist with FDA submission packages.
• Collaborate with Clinical Data Management and Biostatistics teams.
• Maintain programming documentation and standards.

Skills

SAS programming

CDISC/SDTM/ADaM

FDA submissions

Validation practices

Education

Bachelor's degree in Statistics/CS/Math

Job description

Description

SAS Programmer

Venesco is seeking skilled SAS Programmers to develop validated statistical programs and CDISC-compliant datasets to support clinical trials, statistical analyses, safety reporting, and FDA submissions.

Requirements

Duties and Responsibilities

• Develop and validate SAS programs.
• Produce Tables, Listings, and Figures (TLFs).
• Generate SDTM, ADaM, and SEND datasets.
• Develop define.xml files and reviewer guides.
• Create programming validation plans and reports.
• Develop randomization programs and statistical outputs.
• Support interim and final analyses.
• Assist with FDA submission packages.
• Collaborate with Clinical Data Management and Biostatistics teams.
• Maintain programming documentation and standards.

Minimum Qualifications

• Bachelors degree in Statistics, Computer Science, Mathematics, or related field.
• SAS Advanced Programmer Certification required.
• Minimum 7 years of clinical SAS programming experience.
• Extensive experience with CDISC, SDTM, and ADaM standards.
• Experience supporting FDA submissions.
• Strong knowledge of validation practices and regulatory requirements

Venesco, LLC, is an equal opportunity and affirmative action employer. Venesco is committed to administering all employment and personnel actions on the basis of merit and free of discrimination based on race, ethnicity, religious affiliation, gender, gender identity or expression, sexual orientation, national origin, protected veteran status, or status as an individual with a disability. Consistent with this commitment, we are dedicated to the employment and advancement of qualified minorities, women, individuals with disabilities, protected veterans, persons of all ethnic backgrounds and religions according to their abilities.

For more information on Venesco, LLC., visit https://venesco.com.