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Remote Sas Programmer Associate Jobs (NOW HIRING)

AceStack LLC

SAS Admin Remote Contract

SAS Admin Location: Remote (Boston, MA) Long Term Contract - W2/C2C Job Overview: We are seeking an ... Collaborate with developers, analysts, and infrastructure teams to support business needs. * Manage ...

AceStack LLC

SAS Admin Remote Contract

Role: SAS Admin Location: Remote (Boston, MA) Long Term Contract - W2/C2C Job Overview: We are ... Collaborate with developers, analysts, and infrastructure teams to support business needs. * Manage ...

DLH

Research Analyst (SAS and R) (Job 1368)

$50K - $70K/yr

This position is 100% remote . However, employees may be required to attend occasional in-person ... set, SAS programming, and output files. * Conduct geospatial and molecular HIV analysis and ...

Cytel

Principal Statistical Programmer FSP

... advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.

WCG Clinical

Senior Statistical Programmer (Remote)

$73K - $105K/yr

Cary, NC, Remote Organization: ACI Clinical Job Type: Full Time - Regular Description and ... The Senior Statistical Programmer develops, validates, and documents SAS programs to support ...

Slipstream IT

Statistical Analytical Programmer

PA · On-site +1

This person will bring strong SAS programming experience and a practical understanding of ... Able to work independently in a remote environment and manage timelines effectively. Preferred ...

Slipstream IT

Statistical Analytical Programmer

PA · Remote

This person will bring strong SAS programming experience and a practical understanding of ... Able to work independently in a remote environment and manage timelines effectively. Preferred ...

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How much do remote sas programmer associate jobs pay per hour?

As of Jun 27, 2026, the average hourly pay for remote sas programmer associate in the United States is $49.00, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $61.54 per hour, depending on experience, location, and employer.
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Senior Statistical Programmer Analyst Contractor - Remote in US

Senior Statistical Programmer Analyst Contractor - Remote in US

Arcus Biosciences

Remote

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Summary

The Senior Statistical Programmer Analyst Contractor will be responsible for supporting the submission readiness of study data packages per CDISC standards and FDA guidance, planning, execution, and quality of statistical analyses, and statistical programming infrastructure. This position will report into Head of Statistical Programming and will interact regularly with internal and external biostatisticians, clinical data managers, and other team members. Demonstrated ability to prioritize work and to effectively communicate and collaborate with key stakeholders both within Biometrics and beyond (research, translational science, clinical science, clinical operations and regulatory) is a must.


This is a unique opportunity to join a small but growing Biometrics team investigating a diverse portfolio of immuno-oncology therapeutics in early development. The ideal candidate will be a highly experienced technical SAS programmer/developer with an in‐depth understanding of clinical and/or statistical programming processes, tools, systems, and strong communication skills.

Responsibilities

  • Develop specifications, build and execute programs for internal data reviews, publications, exploratory, post-hoc and regulatory review.
  • Adopts strategic approach to producing and prioritizing analytical deliverables which includes study level or integrated analysis for safety signal detection or other business needs.
  • Work with data management to review case report forms, database specifications, and data transfer specifications
  • Manage on-time and quality delivery of CRO-generated analyses results.
  • Solid, demonstrated experience with CDASH and CDISC data standards (SDTM, ADaM) as well as health authority reporting requirements.
  • In-depth knowledge of data standards and demonstrated experience in the handling non-CRF data including proven ability to work with diverse data types.
  • Responsible for creating/reviewing SDTM/ADaM mapping specifications.
  • Generates or validates SDTM domains, ADaM datasets, reviewer's guide, and define.xml files.
  • Generates or validates TFLs to support the statistical analysis of data for clinical studies, regulatory submissions, and publications such as CSR, DSUR, IB, publications, etc. 

Qualifications 

  • Bachelor’s or Master’s degree in a data science field, e.g., statistics, mathematics, epidemiology, computer science, bioinformatics, or another field with commensurate levels of experience
  • 8+ years programming experience with growing responsibility in biotechnology or pharmaceutical clinical trial environment.
  • Experience in software development and testing (e.g., SAS Macros tools, R functions/packages, Unix scripts etc).
  • Experts in developing applications using various technical stacks not limited to SAS, R and/or Python.
  • Solid understanding of industry standards such as CDISC, specifically SDTM and controlled terminology and/or ADaM.
  • Proven ability to translate sophisticated problems into clear and concise programming code/tools.
  • Basic Project management skills and experience.
  • Solid understanding of programming practices (including tools and processes), relevant health authority guidelines, such as (e.g., ICH‐GCP, 21 CFR Part 11), and relevant clinical R&D concepts.
  • Demonstrated strong written, verbal communication skills, ability to manage conflicting demands and priorities and to negotiate successfully.
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