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Senior Clinical Sas Programmer Jobs (NOW HIRING)

VENESCO, LLC

SAS Programmer

Fort Detrick, MD

$135K - $148K/yr

Collaborate with Clinical Data Management and Biostatistics teams. * Maintain programming ... SAS Advanced Programmer Certification required. * Minimum 7 years of clinical SAS programming ...

VENESCO LLC

SAS Programmer

Frederick, MD · On-site

$135K - $148K/yr

Collaborate with Clinical Data Management and Biostatistics teams. * Maintain programming ... SAS Advanced Programmer Certification required. * Minimum 7 years of clinical SAS programming ...

TekCommands Inc

SAS Programmer Lead

North Wales, PA · On-site

Mandatory Skills   SDTM, Clinical SAS JD  Looking for SDTM experts having in-depth knowledge of SAS programming(macro's) 1.Must have 10+ yrs of exp in clinical domain 2.Strong knowledge of ...

Clinical Ink

SAS Programmer

Company Information Clinical Ink is the global life science company that brings data, technology ... Clinical Ink is seeking a SAS Programmer to join our Data Management team based remotely across the ...

VENESCO LLC

SAS Programmer

Falls Church, VA · On-site

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 ...

VENESCO, LLC

SAS Programmer

Falls Church, VA · On-site +1

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 ...

Venesco LLC

SAS Programmer

Falls Church, VA · On-site

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 ...

Tech Tammina LLC

Senior SAS Programmer

Okemos, MI · On-site

Senior SAS Programmer Location: Hybrid - Okemos, MI (Minimum 2 days onsite weekly; moving to 3 days/week soon) · We are looking for a Senior SAS Programmer to join our Data Insights Team. Will work ...

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How much do senior clinical sas programmer jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for senior clinical sas programmer in the United States is $54.05, according to ZipRecruiter salary data. Most workers in this role earn between $40.38 and $61.30 per hour, depending on experience, location, and employer.

What is a senior clinical SAS programmer?

A Senior Clinical SAS Programmer is a specialized professional who uses SAS (Statistical Analysis System) software to manage, analyze, and report clinical trial data in pharmaceutical, biotechnology, or contract research organizations. They are responsible for developing, validating, and maintaining programs that transform raw clinical data into statistical tables, listings, and figures (TLFs) for regulatory submissions and study reports. In addition to technical programming tasks, senior SAS programmers often review code from junior programmers, ensure compliance with regulatory standards, and collaborate with statisticians, data managers, and clinical teams. Their expertise is critical for ensuring data integrity and supporting the success of clinical research projects.

What are the key skills and qualifications needed to thrive as a senior clinical SAS programmer?

To thrive as a Senior Clinical SAS Programmer, you need advanced proficiency in SAS programming, a solid understanding of clinical trial data, and typically a degree in statistics, computer science, or a related field. Expertise in CDISC standards (SDTM, ADaM), experience with clinical data management systems, and familiarity with regulatory submission requirements are essential technical qualifications. Strong analytical thinking, attention to detail, and effective communication skills help in collaborating with cross-functional teams and ensuring data quality. These skills ensure accurate data analysis, compliance with regulatory standards, and successful support of clinical research objectives.

What are some typical challenges faced by senior clinical SAS programmers when managing multiple clinical trial projects simultaneously?

Senior Clinical SAS Programmers often juggle multiple projects at various stages, which can present challenges such as prioritizing tasks, meeting tight regulatory deadlines, and ensuring data quality across studies. Effective communication and collaboration with statisticians, data managers, and clinical teams are essential to address emerging issues quickly. Familiarity with regulatory submission standards and proven organizational skills help in managing the workflow and maintaining consistency in deliverables.
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Senior Clinical Sas Programmer jobs near you
Infographic showing various Senior Clinical Sas Programmer job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $112,418 per year, or $54 per hour.

Senior Clinical SAS Programmer

Katalyst CRO

Philadelphia, PA • On-site

Full-time

Re-posted 8 days ago

Job description

Job Summary:
Katalyst CRO is seeking a Senior Clinical SAS Programmer who will represent the programming function in multi-disciplinary team meetings. The role involves developing CDISC-compliant datasets and documentation for regulatory submissions, as well as creating software systems for clinical study data displays.
Responsibilities:
• Developing CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies.
• Creating or reviewing software systems to generate displays of clinical study data as tables, listings, and graphs for electronic submission to regulatory agencies.
• Assisting statisticians by suggesting algorithms to address client analysis requests.
• Developing software validation procedures and test plans
Qualifications:
Required:
• Minimum years of experience in developing software for clinical trials using the SAS system.
• Skilled in programming with SAS. Knowledge of additional programming languages a plus.
• Good knowledge of statistics and drug development process.
• Experience as a lead programmer for NDAs/BLAs.
• Experience overseeing the work of internal contractors and external vendors (CROs).
Company:
Katalyst CRO | Advancing Healthcare & Life Sciences with Expert Research & Regulatory Solutions Katalyst Healthcare & Life Sciences (Katalyst CRO) is a Global Contract Research and Knowledge Process Outsourcing Organization (CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide. Founded in , the company is headquartered in South Plainfield, USA, with a team of 51-200 employees. The company is currently Growth Stage.

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