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Clinical Sas Jobs (NOW HIRING)

CICONIX, LLC

SAS Programmer

Fort Detrick, MD

SAS Programmer About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in ... Develop statistical programming specifications (clinical data) and other statistical programs used ...

CICONIX, LLC

SAS Programmer

Frederick, MD · On-site

$70 - $90/hr

SAS Programmer About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in ... Develop statistical programming specifications (clinical data) and other statistical programs used ...

DLH

Research Analyst (SAS and R) (Job 1368)

OR · On-site +1

$50K - $70K/yr

Develop SAS programs for validating surveillance, clinical, or research study data. * Verify that all variables that should be included in the resulting dataset are present in the dataset and ...

New

Tunnell Government Services

SAS Programmer

Bethesda, MD · On-site

Title: SAS Programmer Deliverables: * Prepare, update, and maintain all versions of statistical ... Develop statistical programming specifications (clinical data) and other statistical programs used ...

DLH

Research Analyst (SAS and R) (Job 1368)

$50K - $70K/yr

Develop SAS programs for validating surveillance, clinical, or research study data. * Verify that all variables that should be included in the resulting dataset are present in the dataset and ...

New

SPECTRAFORCE

SAS Programmer

North Chicago, IL

Minimum 6 Years SAS Programming Experience supporting Phase 1-3 clinical trials in CRO or pharmaceutical industry. * Solid understanding of SDTM and ADaM implementation guidance, minimum 4 years of ...

Spectra force

SAS Programmer

North Chicago, IL · On-site

Minimum 6 Years SAS Programming Experience supporting Phase 1-3 clinical trials in CRO or pharmaceutical industry. * Solid understanding of SDTM and ADaM implementation guidance, minimum 4 years of ...

DLH

Programmer Analyst (SAS or R)

OR · On-site +1

$71K - $100K/yr

Develop SAS programs for validating surveillance, clinical, or research study data. * Verify that all variables that should be included in the resulting dataset are present in the dataset and ...

New

Tunnell Government Services

SAS Programmer

Bethesda, MD · On-site

SAS Programmer Deliverables: * Prepare, update, and maintain all versions of statistical analysis ... Develop statistical programming specifications (clinical data) and other statistical programs used ...

Collabera

SAS Programmer

Jersey City, NJ · On-site

This position performs statistical programming for clinical studies, integrated summaries, and in ... with SAS in a pharmaceutical or CRO environment Bachelor's Degree or above in Statistics ...

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Clinical Sas information

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$19

$54

$80

How much do clinical sas jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical sas in the United States is $54.04, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $68.03 per hour, depending on experience, location, and employer.

What is a clinical SAS?

Clinical SAS professionals are specialists who use SAS (Statistical Analysis System) software to manage, analyze, and report clinical trial data in the pharmaceutical, biotechnology, and healthcare industries. They play a critical role in ensuring data integrity and compliance with regulatory standards by generating statistical reports, tables, listings, and graphs for clinical studies. These professionals often collaborate with biostatisticians, clinical researchers, and data managers to support the drug development and approval process.

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

To thrive as a Clinical SAS Programmer, you need expertise in SAS programming, a solid understanding of clinical trial data, and a degree in life sciences, statistics, or a related field. Familiarity with CDISC standards (SDTM/ADaM), clinical data management systems, and regulatory submission requirements is typically required. Strong analytical thinking, attention to detail, and effective communication skills set top performers apart in this role. These skills ensure accurate data analysis and reporting, which are critical for regulatory compliance and successful clinical trial outcomes.

What are some common challenges faced by clinical SAS programmers when working on clinical trial data?

Clinical SAS programmers often encounter challenges such as managing large and complex datasets from multiple sources, ensuring strict compliance with regulatory standards (like CDISC, SDTM, and ADaM), and meeting tight project deadlines. They must also collaborate closely with biostatisticians, data managers, and clinical teams to ensure data accuracy and consistency. Staying updated with evolving industry standards and software updates is crucial, as is maintaining clear documentation to support regulatory submissions.

What is the difference between Clinical Sas vs Clinical Data Manager?

AspectClinical SasClinical Data Manager
Required CredentialsBiostatistics, SAS certification, or related trainingBiostatistics, data management certifications, or related degrees
Work EnvironmentStatistical analysis, programming, and reporting in clinical trialsData collection, validation, and database management in clinical studies
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, research organizations

Clinical Sas professionals focus on statistical analysis and programming using SAS software to interpret clinical trial data. In contrast, Clinical Data Managers oversee data collection, validation, and database management to ensure data quality. Both roles are essential in clinical research but differ in their core responsibilities and skill sets.

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Clinical Sas jobs near you
Infographic showing various Clinical Sas job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $112,399 per year, or $54 per hour.

SAS Programmer

CICONIX, LLC

Fort Detrick, MD

Full-time

Medical, Retirement, PTO

Re-posted 14 days ago

Job description

SAS Programmer
About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in business advisory and technical assistance for military health programs. We value exceptional people, unwavering integrity, inclusive collaboration, and enduring impact. 
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Location(s): Fort Detrick, MD
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Position Details:
  • Full-time position
  • Regular weekly hours (0900-1600)
  • No calls, nights, weekends, or holidays!
  • Full benefit program, including: health, PTO, & 401k + contribution
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Requirements:
  • TBD
 
 
Summary:
CICONIX is seeking a SAS Programmer to support the Office of Regulated Activities (ORA) in support of the Defense Health Agency Research and Development Medical Research and Development Command (DHA R&D MRDC) team in Fort Detrick, MD.
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About the Role:
  • Prepare, update, and maintain all versions of statistical analysis plans.
  • Prepare, update, and maintain all versions of Statistical Programming Validation Plans, and all versions of statistical programming validation reports; Develop and provide statistical program formats used in the statistical programs (all versions).
  • Prepare, update, and maintain all versions of randomization plans including randomization list(s) and key(s), prepare statistical programs used to create randomization list(s) and key(s).
  • Develop statistical programming specifications (clinical data) and other statistical programs used to produce the tables, listings, and figures for studies, all versions used for the Data Monitoring Committee, safety surveillance plans, FDA annual report, interim analyses (if applicable), and any ad hoc analyses.
  • Produce data-populated tables, listing, and figures for studies, the Data Monitoring Committee, safety surveillance plans, FDA annual reports, interim analyses (if applicable), and any ad hoc analyses.
  • Develop and revise as required statistical programming specifications used to create CDISC-compliant datasets, SDTM, Analysis Data Model datasets, and Standard for Exchange of Nonclinical Data (SEND) (for non-clinical data); Develop define.xml and define.pdf to include coding conventions used in the statistical programs (all versions) for CDISC datasets; Develop SEND datasets conforming to CDISC standards (non-clinical data); Develop SDTM datasets conforming to CDISC standards; Develop Analysis Data Model datasets conforming to CDISC standards as required.
  • Develop and update as required by CDISC Reviewer’s Guides.
  • Provide written responses to sponsor and FDA requests/queries regarding statistical products.
Qualifications:
  • Education:
    • TBD
  • Licensure & Certifications (Current & Unrestricted): 
    • TBD
  • Experience: 
    • TBD
  • Security & Background Check: 
    • U.S. Citizenship and a successful background investigation are required.
    • Ability to obtain and maintain a government security clearance. 
  • Additional Requirements:
    • Willingness to comply with the government vaccination requirements.
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Compensation: TBD
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*This position is contingent and will begin upon contract award.
CICONIX LLC is an Equal Opportunity Employer, including disability/vets. We E-Verify all employees.
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