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Clinical Sas Programmer Jobs in Reston, VA (NOW HIRING)

ADVI Health LLC

Biostatistician II

Washington, DC · On-site

$140K - $180K/yr

... and clinical trials, applying advanced causal inference methods to generate credible, decision ... Demonstrated programming skills in SAS (required), R (optional) or Python (optional), including ...

ADVI Health LLC

Biostatistician I

Washington, DC · On-site

$112K - $140K/yr

... and clinical trials, applying advanced causal inference methods to generate credible, decision ... Develop and maintain advanced SAS programming workflows to support efficient, reproducible analysis ...

ADVI Health

Senior Data Scientist-RWE

Washington, DC · On-site

$126K - $158K/yr

... SAS programming experience. • 7+ years of experience (or equivalent graduate-level research ... or clinical trial data). • Solid understanding of health outcomes, cost analyses, and study ...

GLOTECH, Inc

Biostatisticians

Rockville, MD · On-site

... clinical trials, and epidemiological studies that explore health processes; examines the impact of ... Develops code in SAS, R, MPlus, SPSS & Stata * Provides analytic programming support for all phases ...

GLOTECH, Inc

Biostatisticians

Rockville, MD · On-site

... clinical trials, and epidemiological studies that explore health processes; examines the impact of ... Develops code in SAS, R, MPlus, SPSS & Stata * Provides analytic programming support for all phases ...

Alpha Omega Integration

Public Health Analyst

Vienna, VA · Remote

$57K - $70K/yr

... SAS will manage and analyze quantitative epidemiological, clinical and/or behavioral data and ... programmer) or by generating cross-tabulations of the variables comprising analysis variables.

Alpha Omega Integration

Public Health Analyst

Vienna, VA · On-site

$57K - $70K/yr

... SAS will manage and analyze quantitative epidemiological, clinical and/or behavioral data and ... programmer) or by generating cross-tabulations of the variables comprising analysis variables.

Alpha Omega Integration

Scientific Data Analyst

Vienna, VA · On-site

$85K - $115K/yr

In this role, you will manage and analyze quantitative epidemiological, clinical and/or behavioral ... SAS code known to be valid for creating the variable (e.g., from past cycles or another programmer ...

Intone Networks

Lead DevOps Engineer

Washington, DC

$56.25 - $77/hr

Intone also offers consulting services in SAS (Clinical Trials), Cloud Computing, CRM, ERP, ... Title: DevOps Engineer Location: Washington, DC Duration: 6 Month contract to hire MUST HAVE

Intone Networks

Lead DevOps Engineer

Washington, DC · On-site

$56.25 - $77/hr

Intone also offers consulting services in SAS (Clinical Trials), Cloud Computing, CRM, ERP, ... Title: DevOps Engineer Location: Washington, DC Duration: 6 Month contract to hire MUST HAVE

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Clinical Sas Programmer information

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How much do clinical sas programmer jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for clinical sas programmer in Reston, VA is $56.22, according to ZipRecruiter salary data. Most workers in this role earn between $43.27 and $70.77 per hour, depending on experience, location, and employer.

How much do SAS programmers make?

SAS programmers typically earn between $70,000 and $120,000 annually, depending on experience, location, and industry. Senior or specialized SAS programmers with certifications and extensive skills can earn higher salaries, especially in pharmaceutical or clinical research sectors where SAS is widely used for data analysis and reporting.

What is a Clinical SAS Programmer?

A Clinical SAS Programmer is a professional who uses SAS (Statistical Analysis System) software to manage, analyze, and report clinical trial data in the pharmaceutical, biotechnology, and medical research industries. Their main responsibilities include creating programs to clean, organize, and analyze clinical data, generating summary tables and listings, and ensuring the accuracy and compliance of data for regulatory submissions. They work closely with biostatisticians, data managers, and clinical researchers to support drug development and approval processes.

Is clinical SAS programmer a good career?

A clinical SAS programmer is a specialized role in the pharmaceutical and healthcare industries, focusing on data analysis and reporting using SAS software. It offers stable employment opportunities, competitive salaries, and requires skills in programming, biostatistics, and understanding clinical trial processes. Certification and experience can enhance career growth in this field.

How much do entry level clinical SAS programmers make in the US?

Entry-level clinical SAS programmers in the US typically earn between $60,000 and $80,000 annually, depending on location, education, and certifications. Starting salaries may increase with experience, knowledge of clinical trial processes, and proficiency in SAS programming tools.

What are the key skills and qualifications needed to thrive as a Clinical SAS Programmer, and why are they important?

To thrive as a Clinical SAS Programmer, you need strong programming skills in SAS, a solid understanding of clinical trial data, and often a degree in statistics, computer science, or a related field. Familiarity with CDISC standards (SDTM, ADaM), clinical data management systems, and regulatory submission processes is typically required. Attention to detail, problem-solving abilities, and effective communication skills help you collaborate with cross-functional teams and ensure data quality. These skills are vital for ensuring accurate data analysis and compliance with industry regulations in clinical research.

What is the difference between Clinical Sas Programmer vs Clinical Data Analyst?

AspectClinical Sas ProgrammerClinical Data Analyst
Required CredentialsBachelor's in IT, Life Sciences, or related; SAS certification often preferredBachelor's in Statistics, Data Science, or related; often requires statistical or data analysis certifications
Work EnvironmentPharmaceutical or CRO settings, working with SAS software to develop datasets and reportsResearch or clinical settings, analyzing clinical data to generate insights and reports
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, research organizations, healthcare providers

While both roles involve working with clinical data, Clinical Sas Programmers focus on programming, data manipulation, and report generation using SAS software. Clinical Data Analysts primarily analyze data to interpret results and support decision-making. Both roles require strong analytical skills but differ in their core responsibilities and technical focus.

What are 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, ensuring data integrity, and adhering to strict regulatory guidelines. They must also collaborate closely with biostatisticians and data managers to resolve data discrepancies and interpret study protocols accurately. Timely delivery of high-quality statistical outputs, such as tables, listings, and figures, is critical, often under tight deadlines. Effective communication and attention to detail are essential to overcome these challenges and deliver reliable results.

What is the salary of clinical SAS programmer?

The salary of a clinical SAS programmer typically ranges from $70,000 to $110,000 annually, depending on experience, location, and certifications. Entry-level positions may start lower, while experienced programmers with advanced skills can earn higher salaries, especially in competitive markets or with specialized knowledge of clinical trial data analysis.

What Is a SAS Clinical Programmer?

As a SAS clinical programmer, your primary responsibilities are the management and analysis of large datasets of information from clinical trials. Your job duties include using and programming the statistical analysis system, or SAS software suite, to develop tables and reports about the interdependencies of data points and the efficacy of trial-phase clinical therapies. The qualifications for a career as a SAS clinical programmer are a bachelor’s degree in statistics or computer science and experience in the pharmaceutical or clinical industries. You must develop strong SAS technical skills and problem-solving skills to succeed in a career as a SAS clinical programmer.

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Clinical Sas Programmer jobs near you
Senior Director, Biostatistics

Senior Director, Biostatistics

Supernus Pharmaceuticals, Inc.

Rockville, MD • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago

Job description

Supernus Pharmaceuticals is an award-winning biopharmaceutical company with more than 30 years of experience in developing and commercializing products that treat central nervous system (CNS) diseases. At Supernus, we develop innovative products that help treat neurological and psychiatric conditions. At Supernus, we develop innovative products that help treat neurological and psychiatric conditions. We currently have 8 products in the market that are making a real impact on patient outcomes.
Job Summary:
To contribute to the Company's Clinical program by providing direction, insight, and hands-on management & leadership covering the statistical content and requirements for Phase 1 through 4 activities.
Essential Duties & Responsibilities:
  • Provides statistical support and expertise for all necessary activities in Development, specifically design of Phase 1-4 studies and programs.
  • Provides for the statistical content of clinical trials.
  • Provides team leadership for regulatory filings including integrated components.
  • Provides hand-on supports to all statistical deliverables.
  • Provides statistical leadership and insight to team as a senior member of the Clinical Development organization.
  • Interacts with FDA and other regulatory agencies in statistical aspects of study design and data analysis.
  • Works under limited supervision.
  • Assists with other duties as needed by the management.

Supervisory Responsibilities:
  • Builds statistical group (including the hiring of new staff and development of existing staff) in an efficient manner to accomplish corporate objectives and elevate overall statistical group's performance.
  • Leads and/or manages both in-house and CRO activities related to application of statistics to clinical trials data.
  • Leads in the development and review of SOPs related to statistics.
  • Provides leadership and management in an effective manner consistent with Company Values towards defined Corporate Objectives.
  • Understands Company Policy and procedure to be able to guide direct reports appropriately.

Knowledge & Other Qualifications:
  • PhD (or equivalent) in Statistics or Biostatistics.
  • Excellent presentation, communication and management skills with attention to detail and accuracy.
  • 10+ years of pharmaceutical industry experience (6+ years in a pharmaceutical company or regulatory agency).
  • Major participation as the statistical lead in at least 1 NDA filing.
  • Proven ability to help design successful clinical trials.
  • Proven ability to independently develop and lead statistical components of several ongoing projects in Phase 1-4.
  • Proven ability to lead adaptive design, longitudinal data analysis, missing data handling and sensitivity analysis.
  • Experience with PK and PK/PD methods and clinical trial simulation a plus.
  • Fluent in SAS programming (including SAS macro) and familiarity with other statistical packages (e.g., PASS, nQuery Advisor, R).
  • Expert knowledge of FDA guidance related to statistics and statistical programming.
  • Knowledge of ICH/GCP rules and regulations.
  • Must be able to clearly articulate project needs and status to project team and upper management.
  • Excellent interpersonal and communication skills in English language (writing, speaking, comprehending).
  • Computer literate with proficiency of Microsoft Office package including Word, Outlook, Excel, and Adobe PDF.

Other Characteristics:
  • Ability to work independently and as part of a team and maintain high ethical standards of integrity and quality.
  • Ability to lead and manage direct reports and statistical group.
  • Ability of having an innovative and dynamic approach to work.
  • A self-starter able to work independently and also comfortable working in a team environment.
  • Ability to consistently exhibit Supernus Values in interactions with employees at all levels of the organization, vendors, customers and others.
  • Capable of performing other duties as assigned by Management.
  • Authorized to legally work in the United States without visa sponsorship.

Physical Requirements/Work Environment/Travel Requirements:
  • Sedentary work. Exerting up to 10 pounds of force occasionally and/or carrying objects. Sedentary work involves sitting most of the time.
  • The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer screen, iPad, or other electronic device; and extensive reading.
  • The worker is not substantially exposed to adverse environmental conditions.

Compensation:
At Supernus, we offer a competitive compensation package that reflects your experiences and contributions. The expected salary range for fully qualified candidates applying for this role is $257,000 to $294,000. This range is what the Company reasonably expects to offer for the position and is not reflective of the full compensation scale of the role. This range may be modified in the future. An individual's salary within the range is based on multiple factors, which may include and are not limited to education, relevant experience, knowledge, length of industry experience and organizational needs.
You also will be able to participate in a competitive benefits package, including but not limited to: health, dental, vision, paid time off, 401k company match, company paid life insurance and health and wellness benefits. The total compensation package for this position also includes other compensation elements such as stock equity awards, employee stock purchase programs and participation in our Company's discretionary annual bonus program.
Supernus Pharmaceuticals is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, disability, protected veteran status, age or any other characteristic protected by law.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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