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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 ...

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 · 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.

SystImmune, Inc.

$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 ...

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 ...

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

Fort Detrick, 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.

VENESCO LLC

SAS Programmer

Fort Detrick, 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.

Solomon Page

Sr. Statistical Programmer

Princeton, NJ · On-site

$75 - $80/hr

The Senior Statistical Programmer plays a critical role in supporting clinical development programs ... CDISC-compliant SDTM datasets * ADaM datasets * Tables, Listings, and Figures (TLFs) * Patient ...

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

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

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

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SDTM Programmer information

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How much do sdtm programmer jobs pay per hour?

As of Sep 11, 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 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.

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.

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SDTM Programmer jobs near you
Infographic showing various Sdtm Programmer job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 50% In-person, and 50% Remote job distribution, with an average salary of $82,234 per year, or $39.5 per hour.

Clinical SAS Programmer

Newark, NJ

Katalyst Healthcares & Life Sciences
Scientific Research and Development Services • 51 - 200 employees
Learn more about Katalyst Healthcares & Life Sciencesexternal

Contractor

Re-posted 23 days ago

Job description

Company Description
  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.
Job Description

Responsibilities:

  • Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s).
  • Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets.
  • Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements.
  • Provides input in the design and development of case report forms and clinical databases.
  • Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs.
  • Programs for quality checks for clinical study raw data and report the findings to Data Management.
  • Provides input in the design and development of case report forms and clinical study databases.
  • Reviews or author aCRF, SDTM and ADaM datasets specifications for datasets programming.

Requirements:

  • MS in Statistics, Computer Science, or a related field with at least 3 years or BS in Statistics, Computer Science, or a related field with at least 5 years.
  • Experience in providing statistical programming support to early and late phase clinical trials.
  • Excellent skills in SAS programming and statistical reporting.
  • Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements.
  • Familiarity with FDA and ICH regulations and guidelines.
  • Excellent problem-solving skills.
  • Good written and verbal communication skills and organizational and documentation skills.
  • Ability to work on a multidisciplinary team that may include Biostatistics, Medical Directors, Data Management, Medical Writing, Pharmacovigilance, Clinical Operations, Medical Affairs, etc.
  • Ability to prioritize and multi-task effectively.
  • Demonstrated positive attitude and the ability to work well with others.
Additional Information

All your information will be kept confidential according to EEO guidelines.

Katalyst Healthcares & Life Sciences logo

About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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