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Clinical R Programmer Jobs in Washington (NOW HIRING)

TRI Challenge Convention

Statistician

Bethesda, MD · On-site

Minimum of 3-5 years of experience in a CRO environment Demonstrated proficiency with statistical methods and applications in clinical research Strong programming skills in SAS and/or R. Ability to ...

Otsuka

Associate Director, Biostatistics

Rockville, MD · On-site +1

... phase clinical data. Skills * In-depth knowledge of statistical principles, applications, and SAS/R programming software. * Strong computer skills with demonstrated experience in working with the ...

Otsuka

Associate Director, Biostatistics

Rockville, MD · On-site +1

... and clinical operation. * Familiar with regulatory submission process in US and EU. Skills * In-depth knowledge of statistical principles, applications, and SAS/R programming software. * Strong ...

To The Moon

BCBA Clinical Supervisor

Woodbridge, VA · On-site

$73K - $89K/yr

Conduct skills assessments including ABLLS-R, ABAS, VB-MAPP, Vineland, PEAK or AFLS assessment ... Provide oversight to Behavior Technicians, including monitoring the implementation of programming ...

To The Moon

BCBA Clinical Supervisor

Fairfax, VA · On-site

$76K - $93K/yr

Conduct skills assessments including ABLLS-R, ABAS, VB-MAPP, Vineland, PEAK or AFLS assessment ... Provide oversight to Behavior Technicians, including monitoring the implementation of programming ...

To The Moon

BCBA Clinical Supervisor

Springfield, VA · On-site

$77K - $95K/yr

Conduct skills assessments including ABLLS-R, ABAS, VB-MAPP, Vineland, PEAK or AFLS assessment ... Provide oversight to Behavior Technicians, including monitoring the implementation of programming ...

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Clinical R Programmer information

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

To thrive as a Clinical R Programmer, you need a solid background in statistics, R programming, and clinical trial data analysis, often supported by a degree in statistics, biostatistics, or a related field. Expertise in SAS, CDISC standards (SDTM/ADaM), and familiarity with clinical data management systems are commonly required. Attention to detail, problem-solving skills, and effective communication enable you to interpret data accurately and collaborate with cross-functional teams. These skills are vital for ensuring reliable statistical outputs that support regulatory submissions and data-driven decisions in clinical research.

What are some common challenges faced by Clinical R Programmers when working with clinical trial data?

Clinical R Programmers often encounter challenges such as handling large and complex datasets, ensuring strict compliance with regulatory standards (like CDISC SDTM and ADaM), and maintaining data integrity throughout the analysis process. Collaboration can be demanding, as programmers must frequently coordinate with biostatisticians, data managers, and clinical teams to interpret data requirements and resolve discrepancies. Staying updated with evolving industry guidelines and managing tight project timelines are also common aspects of the role.

What are Clinical R Programmers?

Clinical R Programmers are professionals who use the R programming language to manage, analyze, and visualize clinical trial data in the pharmaceutical, biotech, or healthcare industries. They play a key role in preparing statistical reports, generating tables, listings, and figures (TLFs), and ensuring data integrity for regulatory submissions. Clinical R Programmers collaborate with statisticians, data managers, and clinical teams to ensure the accuracy and compliance of clinical trial results with industry standards and regulatory requirements.

What is the difference between Clinical R Programmer vs Clinical SAS Programmer?

AspectClinical R ProgrammerClinical SAS Programmer
Required CredentialsTypically requires a degree in statistics, biostatistics, or related field; proficiency in R programmingUsually requires a degree in statistics, biostatistics, or related field; proficiency in SAS programming
Work EnvironmentOften works in research-focused settings, academia, or biotech companies using open-source toolsCommonly employed in pharmaceutical companies, CROs, and clinical trial data analysis using SAS
Industry UsageGrowing in popularity for data analysis and visualization in clinical researchStandard in clinical trial data management and regulatory submissions

While both roles involve programming for clinical data analysis, Clinical R Programmers focus on using R for statistical analysis and visualization, whereas Clinical SAS Programmers primarily use SAS for data management and reporting. The choice depends on the company's preferred tools and project requirements.

What are popular job titles related to Clinical R Programmer jobs in Washington? For Clinical R Programmer jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Clinical R Programmer jobs in Washington look for? The top searched job categories for Clinical R Programmer jobs in Washington are:
What cities in Washington are hiring for Clinical R Programmer jobs? Cities in Washington with the most Clinical R Programmer job openings:
Clinical R Programmer jobs near you

Clinical SAS Programmer

Interon IT Solutions

Chantilly, VA • Remote

Contractor

Posted 25 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.