Key Facts

Remote From:

Full time

Senior (5-10 years)

English

Hard Skills

SAS (Software) SAS (Software) Regulatory Compliance Clinical Data Analysis Software Documentation Auditing Data Validation FDA Regulations Python (Programming Language)

Other Skills

•
Teamwork
•
Collaboration

Roles & Responsibilities

Bachelor's or Master's degree in Statistics or a related field
5+ years of SAS programming experience in clinical research
Experience with CDISC standards (SDTM and ADaM)
Experience supporting FDA submissions

Requirements:

Develop SAS programs for tables, listings, and figures (TLFs)
Create CDISC-compliant datasets (SDTM and ADaM)
Validate and document programming outputs
Support regulatory submissions and audits

Venesco, LLC

Aerospace & Defense

About Venesco, LLC

We have evolved over the past 18 years, starting as a small consulting business and emerging as a well-respected business specializing in biomedical R&D and IT support services. Our success on federal initiatives is the product of our distinguished professional employees, agile management & quality processes, and financial aptitude. We have solid financials and mature processes, backed by our recognition in Inc. 5000 and Washington Technology's Fast 50 in 2017, 2018, 2019, 2020, and 2021. We possess a Top-Secret Facility Clearance and hold certifications for CMMI® Maturity Level 3 (ML3) for services and ISO 9001:2015 and 14001:2015. Our 14 prime multiple-award IDIQ contracts have yielded a wealth of expertise in program, task order, and contract management worldwide. Venesco runs 65+prime contracts, ranging in size from as few as one or two employees to programs with 150+ employees. With over 350 credentialed employees, Venesco is a nimble small business with a large business impact and reach.

Company type: SME

Industry: Aerospace & Defense

Founded: 2018

Company size: 201 - 500

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Job description

Description

SAS Programmer

Location: Remote/Hybrid
Job Type: Full-Time

Position Overview:
Venesco is seeking a skilled SAS Programmer to support clinical data analysis and regulatory submission activities.

Requirements

Key Responsibilities: • Develop SAS programs for tables, listings, and figures (TLFs) • Create CDISC-compliant datasets (SDTM and ADaM) • Validate and document programming outputs • Collaborate with statisticians and data management teams • Support regulatory submissions and audits

Minimum Qualifications: • Bachelor’s or Master’s degree in Statistics or related field • 5+ years of SAS programming experience in clinical research • Experience with CDISC standards

Preferred Qualifications: • Experience supporting FDA submissions • Knowledge of Python

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