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Sdtm Programmer Jobs (NOW HIRING)

SystImmune, Inc

Statistical Programmer

Redmond, WA · On-site

$80K - $100K/yr

The Statistical Programmer will support statistical programming activities for clinical trials ... Generate and/or validate SDTM and ADaM datasets, including associated Define.xml and reviewer ...

VENESCO, LLC

SAS Programmer

Fort Detrick, MD

$135K - $148K/yr

Generate SDTM, ADaM, and SEND datasets. * Develop define.xml files and reviewer guides. * Create programming validation plans and reports. * Develop randomization programs and statistical outputs.

Systimmune

Statistical Programmer

Redmond, WA · On-site

$80K - $100K/yr

The Statistical Programmer will support statistical programming activities for clinical trials ... Generate and/or validate SDTM and ADaM datasets, including associated Define.xml and reviewer ...

VENESCO LLC

SAS Programmer

Frederick, MD · On-site

$135K - $148K/yr

Generate SDTM, ADaM, and SEND datasets. * Develop define.xml files and reviewer guides. * Create programming validation plans and reports. * Develop randomization programs and statistical outputs.

Fortrea

$80K - $95K/yr

... programming or Visual Analytics tools like Spotfire or Tableau ... Develop/validate Custom/Complex SAS / SDTM datasets and efficiently handle external data and ...

Fortrea

Senior Programmer Analyst

Durham, NC · On-site

$80K - $95K/yr

... programming or Visual Analytics tools like Spotfire or Tableau ... Develop/validate Custom/Complex SAS / SDTM datasets and efficiently handle external data and ...

Fortrea

Senior Programmer Analyst

Durham, NC · Remote

$80K - $95K/yr

... programming or Visual Analytics tools like Spotfire or Tableau ... Develop/validate Custom/Complex SAS / SDTM datasets and efficiently handle external data and ...

VENESCO LLC

SAS Programmer

Falls Church, VA · On-site

Create CDISC-compliant datasets (SDTM and ADaM) * Validate and document programming outputs * Collaborate with statisticians and data management teams * Support regulatory submissions and audits ...

VENESCO, LLC

SAS Programmer

Falls Church, VA · On-site +1

Develop SAS programs for tables, listings, and figures (TLFs) Create CDISC-compliant datasets (SDTM and ADaM) Validate and document programming outputs Collaborate with statisticians and data ...

Venesco LLC

SAS Programmer

Falls Church, VA · On-site

Requirements Key Responsibilities: • Develop SAS programs for tables, listings, and figures (TLFs) • Create CDISC-compliant datasets (SDTM and ADaM) • Validate and document programming outputs ...

CICONIX, LLC

SAS Programmer

Fort Detrick, MD · On-site

SAS Programmer About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in ... Develop SDTM datasets conforming to CDISC standards; Develop Analysis Data Model datasets ...

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How much do sdtm programmer jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for sdtm programmer in the United States is $39.54, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $51.44 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the SDTM programmer position, and why are they important?

To thrive as an SDTM Programmer, you need a strong background in clinical data management, data standards (especially CDISC SDTM), and programming skills—typically in SAS. Familiarity with SDTM mapping, data validation tools, and relevant regulatory submission platforms or certifications (e.g., SAS Certified Clinical Trials Programmer) is highly valuable. Strong attention to detail, analytical thinking, and effective communication enable collaboration with clinical teams and accurate data interpretation. These skills ensure clinical trial data is accurately standardized, regulatory-compliant, and ready for analysis, which is critical to successful drug development processes.

What is an SDTM programmer?

An SDTM Programmer is responsible for converting clinical trial data into standardized Study Data Tabulation Model (SDTM) datasets as per CDISC (Clinical Data Interchange Standards Consortium) guidelines. They ensure that data is structured and formatted correctly for regulatory submissions to agencies like the FDA or EMA. Their work involves writing SAS programs, validating datasets, and collaborating with clinical teams to ensure compliance and accuracy. Strong knowledge of SDTM standards, SAS programming, and clinical trial processes is essential for this role.

What are the typical daily responsibilities of an SDTM programmer?

SDTM Programmers are primarily responsible for transforming raw clinical trial data into standardized SDTM domains using programming languages like SAS. On a daily basis, you may be involved in mapping study data to SDTM specifications, validating the datasets, resolving discrepancies with data management teams, and documenting your processes for regulatory review. Collaboration with biostatisticians, clinical data managers, and quality assurance teams is also a significant part of the role. These responsibilities ensure that clinical data is accurate, compliant with industry standards, and prepared for analysis and submission to regulatory agencies.

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Sdtm Programmer jobs near you
Infographic showing various Sdtm Programmer job openings in the United States as of August 2026, with employment types broken down into 85% Full Time, 5% Part Time, 9% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $82,234 per year, or $39.5 per hour.

Statistical Programmer

SystImmune, Inc

Redmond, WA • On-site

$80K - $100K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 4 days ago

Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
The Statistical Programmer will support statistical programming activities for clinical trials, including generating SDTM/ADaM datasets, tables, figures, and listings (TFLs). This role is ideal for someone early in their career who is eager to learn and grow in a fast-paced biotech environment with exposure to end-to-end clinical development.
This position is full-time onsite at our Redmond, WA location and we will be moving to our new location in Bothell, WA fall 2026. We will consider candidates for our Princeton, NJ location on a case by case basis.
Responsibilities
  • Collaborate with biostatisticians and cross-functional study team members to deliver statistical analysis and reporting outputs in line with project timelines.
  • Review study documents including statistical analysis plans (SAPs), CRFs, database specifications, and data transfer specifications.
  • Create and/or review SDTM/ADaM mapping specifications and annotated CRFs (aCRFs).
  • Generate and/or validate SDTM and ADaM datasets, including associated Define.xml and reviewer's guides.
  • Develop and validate tables, figures, and listings (TFLs) to support clinical study analyses, regulatory submissions, conferences, and publications.
  • Assess the quality, integrity, and consistency of analysis datasets, including cross-study analyses where applicable.
  • Develop SAS programs and macros to automate dataset generation and reporting deliverables.
  • Contribute to process improvements and enhancements of the statistical programming environment.
  • Participate in study team meetings and representing statistical programming in cross-functional discussions.
  • Apply knowledge of clinical trial design, CDISC standards, and regulatory requirements while producing analysis datasets and outputs in compliance with SOPs and industry standards.

Qualifications
  • Master's degree or higher in Biostatistics, Statistics, Mathematics, or a related scientific discipline, with 0-2 years of experience in statistical programming within the pharmaceutical/biotech industry or a CRO.
  • Proficiency in SAS programming, preferably with experience in a clinical trial environment.
  • Working knowledge of CDISC standards (SDTM and ADaM).
  • Hands-on experience in developing and validating SDTM and ADaM datasets, as well as statistical outputs (tables, figures, and listings).
  • Prior experience or exposure to oncology studies is preferred.
  • Strong analytical, problem-solving, and organizational skills.
  • Effective communication and interpersonal skills, with the ability to work collaboratively in cross-functional teams.

Compensation and Benefits:
The expected base salary range for this position is $80,000 - $100,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's level qualifications, experience, and skills.
While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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