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Intern Remote Clinical Sas Programmer Jobs in Washington

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 ...

Director of Biostatistics

Alexandria, VA ยท Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological ...

Director of Biostatistics

Washington, DC ยท Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological ...

Internship Program US (Remote)

Bethesda, MD ยท On-site +1

$18 - $23.25/hr

... intern to develop an understanding of how to create value through reducing operating costs in ... Unique skills in energy modeling, Excel, PowerPoint, data analytics, or engineering and design are ...

Analyze and validate clinical trial data. * Review and interpret Statistical Analysis Plans (SAPs ... Perform statistical analyses using SAS and/or R . * Collaborate with cross-functional teams and ...

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Intern Remote Clinical Sas Programmer information

What is an intern remote clinical SAS programmer?

An Intern Remote Clinical SAS Programmer is a trainee who assists in analyzing and managing clinical trial data using SAS software, while working remotely. Typically, this role involves supporting experienced clinical programmers in coding, validating datasets, and generating reports for clinical research studies. Interns gain hands-on experience with clinical data management, statistical programming, and compliance with regulatory standards. This position is ideal for students or recent graduates interested in pharmaceutical research, biostatistics, or data science.

What is the difference between Intern Remote Clinical Sas Programmer vs Clinical SAS Programmer?

AspectIntern Remote Clinical SAS ProgrammerClinical SAS Programmer
CredentialsTypically pursuing or recently completed relevant degree; less experience requiredUsually requires a degree in a related field; more experience preferred
Work EnvironmentRemote internship, often part-time or temporaryFull-time, often remote or on-site in clinical research settings
Employer & Industry UsageUsed by biotech/pharma companies for training and entry-level rolesUsed in clinical research organizations, pharmaceutical companies, and CROs

The main difference is that an Intern Remote Clinical SAS Programmer is an entry-level, often temporary role designed for learning and gaining experience, while a Clinical SAS Programmer is a more experienced professional responsible for developing and maintaining clinical data analysis programs. Interns typically have less experience and work under supervision, whereas Clinical SAS Programmers handle complex tasks independently.

Are SAS programmers in demand?

SAS programmers, including those in clinical and data analysis roles, are in steady demand due to the continued need for data management and statistical analysis in healthcare, pharmaceuticals, and research industries. Skills in SAS programming, along with knowledge of clinical trial processes and regulatory requirements, enhance employability in this field.

What types of projects and responsibilities can I expect as an intern remote clinical SAS programmer?

As a remote clinical SAS programmer intern, you will typically assist in the preparation, validation, and analysis of clinical trial data. Your daily tasks may include writing and debugging SAS code, generating tables, listings, and figures for clinical study reports, and ensuring data compliance with regulatory standards. You'll likely collaborate closely with biostatisticians, data managers, and other programmers, often communicating via virtual meetings and project management tools. This role provides a valuable opportunity to gain hands-on experience with real-world clinical data and to develop technical and collaborative skills essential for future advancement in the pharmaceutical or clinical research industry.

What are the key skills and qualifications needed to thrive as an intern remote clinical SAS programmer, and why are they important?

To thrive as an Intern Remote Clinical SAS Programmer, you typically need a background in statistics, life sciences, or a related field, along with basic proficiency in SAS programming. Familiarity with clinical trial data standards (such as CDISC), statistical analysis software (especially SAS Base and SAS Macro), and regulatory documentation is important. Strong attention to detail, problem-solving abilities, and effective remote communication skills help set you apart in this role. These skills ensure accurate data analysis, regulatory compliance, and effective collaboration within distributed clinical research teams.

What are popular job titles related to Intern Remote Clinical Sas Programmer jobs in Washington?

For Intern Remote Clinical Sas Programmer jobs in Washington, the most frequently searched job titles are:

Infographic showing various Intern Remote Clinical Sas Programmer job openings in Washington as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 18% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Clinical SAS Programmer

Interon IT Solutions

Chantilly, VA โ€ข Remote

Contractor

Re-posted 7 days ago


Job description

#W2 Role

Job Title: Clinical SAS Programmer

No of positions- 2

Location- Remote
Experience Required:6+ Years
Education: Bachelor’s degree in Computer Science, Computer Engineering, or related technical field

 

Job Summary

We are seeking a Clinical SAS Programmer with strong experience in SAS programming and CDISC standards within a regulatory environment. The ideal candidate will be responsible for creating and validating SDTM domains and ADaM datasets, developing mapping specifications, and supporting clinical data programming activities with accuracy and compliance.

Key Responsibilities

  • Develop and validate specifications for creating SDTM domains from raw/source clinical data.
  • Create and validate CDISC-compliant SDTM domains and ADaM datasets using SAS.
  • Prepare mapping specifications from CRF and other raw data sources to appropriate SDTM domains.
  • Develop specifications to map SDTM datasets to ADaM datasets.
  • Write clear and detailed programming instructions for complex data derivations.
  • Perform dataset validation and quality checks to ensure regulatory compliance and data integrity.
  • Develop SAS macros and reusable programs to improve efficiency and streamline workflow.
  • Apply advanced SAS programming techniques for custom clinical data programming needs.
  • Work effectively in a dynamic environment and adapt quickly to changing project requirements.

Required Qualifications

  • Bachelor’s degree in Computer Science, Computer Engineering, or a related technical field.
  • 4+  years of experience in clinical SAS programming.
  • Strong hands-on experience using SAS to create CDISC-compliant outputs in a regulated clinical environment.
  • Solid understanding of SDTM, ADaM, and clinical data standards.
  • Experience in writing and validating dataset specifications.
  • Familiarity with P21 software.
  • Excellent written and verbal communication skills.

Preferred Qualifications

  • Experience with R and Python is a strong plus.
  • Ability to work independently and collaboratively within cross-functional teams.
  • Strong attention to detail and problem-solving skills.