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Sdtm Programmer Jobs in California (NOW HIRING)

Fortrea

Senior Statistical Programmer

San Jose, CA · Remote

Plan, execute and oversee all programming activities on a study, including but not limited to ... Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform QC of SDTM ...

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Sdtm Programmer information

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$11

$39

$67

How much do sdtm programmer jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for sdtm programmer in California is $39.02, according to ZipRecruiter salary data. Most workers in this role earn between $25.38 and $50.77 per hour, depending on experience, location, and employer.

How hard is it to get a job at SAS?

Sdtm Programmers can find opportunities at SAS, especially with strong knowledge of SAS tools, programming skills, and understanding of clinical data standards. Entry-level roles may require relevant certifications or experience, but the hiring process generally depends on the candidate's technical expertise and industry experience. Competition can vary based on location and demand for specialized skills in clinical data management.

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 job?

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.

Is SAS programming in demand?

SAS programming remains in demand, especially in industries like pharmaceuticals, healthcare, and finance that rely on clinical trial data analysis and regulatory reporting. Skilled SAS programmers with knowledge of data management, statistical analysis, and validation tools are sought after, and proficiency in SAS can lead to stable employment opportunities.

What is the role of SDTM programmer?

An SDTM programmer is responsible for developing and validating data tabulation models (SDTM) for clinical trial data submissions, ensuring compliance with regulatory standards such as CDISC. They use programming languages like SAS or R to transform raw data into standardized formats, supporting accurate data analysis and reporting.

How much do SAS programmers make?

SAS programmers, including SDTM programmers who specialize in clinical data management, typically earn between $70,000 and $120,000 annually, depending on experience, location, and certifications. Entry-level positions may start around $60,000, while senior roles with advanced skills and certifications can exceed $130,000. Salary also varies based on the complexity of projects and the industry sector.

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 California as of June 2026, with employment types broken down into 20% Full Time, 33% Part Time, 40% Contract, and 7% Nights. Highlights an 72% Physical, 5% Hybrid, and 23% Remote job distribution, with an average salary of $81,158 per year, or $39 per hour.
Sr. Statistical Programmer

Sr. Statistical Programmer

Redbock - an NES Fircroft company

Hayward, CA

Other

Posted 20 days ago

Job description

SUMMARY:

A biopharmaceutical company in the Bay area needs a very strong Senior Statistical Programmer to support their team. This programmer will need to be a strong, senior-level programmer who can work well both independently and part of a team. They must be proficient in their CDISC expertise and be able to program specifications from scratch (both SDTM and ADaM programming).


DUTIES & RESPONSIBILITIES:

  • Perform data manipulation, analysis and reporting of clinical trial data
  • Program and generate tables, listings, and graphs (TLGs)
  • Participate in the review of statistical analysis plans, table specification, develop specification for SDTM and ADaM data sets.
  • Review, and comment on CRFs, annotated CRFs, and edit checks and related documents.
  • Participate in study team meetings and address issues that may affect statistical programming.
  • Validate and document SAS programs and output
  • Create SDTM and ADaM Datasets and related documentation
  • Fulfill ad-hoc programming requests
  • Other duties as needed


QUALIFICATIONS & REQUIREMENTS:

  • 15+ years of statistical programming experience in the pharmaceutical/biotech industries, good tenure with Sponsor companies
  • Strong submissions experience (BLA, NDA/sNDA and EMA), understanding submission requirements, and end to end programming experience
  • Strong experience with CDISC implementation – SDTM/ADAM, must be able to develop specifications from scratch
  • Demonstrated ability performing all levels of programming activities for a clinical project
  • Experience working in the Cardiovascular or Neuromuscular areas is a plus

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