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Sdtm Programmer Jobs in California (NOW HIRING)

Gilead

Sr Manager, Statistical Programming

Foster City, CA

$169K - $219K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM) * Proven experience in complex and fast turnaround programming activities * Excellent interpersonal, communication, problem solving, and ...

Gilead

Sr Manager, Statistical Programming

Foster City, CA · On-site

$169K - $219K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM) * Proven experience in complex and fast turnaround programming activities * Excellent interpersonal, communication, problem solving, and ...

Exelixis

Senior AI Data Scientist I

Alameda, CA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Leveraging statistical programming (R, Python, SQL) and machine-learning techniques, this role ... Basic familiarity with CDISC data standards (SDTM, ADaM) concepts. * Ability to communicate ...

Exelixis, Inc.

Senior AI Data Scientist I

Alameda, CA · On-site

$143.50 - $203/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Leveraging statistical programming (R, Python, SQL) and machine-learning techniques, this role ... Basic familiarity with CDISC data standards (SDTM, ADaM) concepts.* Ability to communicate ...

Exelixis

Senior AI Data Scientist I

Alameda, CA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Leveraging statistical programming (R, Python, SQL) and machine-learning techniques, this role ... Basic familiarity with CDISC data standards (SDTM, ADaM) concepts. * Ability to communicate ...

Exelixis Inc

Senior AI Data Scientist I

Alameda, CA · On-site

$143.50 - $203/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Leveraging statistical programming (R, Python, SQL) and machine‑learning techniques, this role ... Basic familiarity with CDISC data standards (SDTM, ADaM) concepts. * Ability to communicate ...

Exelixis

Senior AI Data Scientist I

Alameda, CA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Leveraging statistical programming (R, Python, SQL) and machine-learning techniques, this role ... Basic familiarity with CDISC data standards (SDTM, ADaM) concepts. * Ability to communicate ...

Neurocrine Biosciences

Principal Biostatistician

San Diego, CA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... programming statistical analyses commonly used in the analysis of clinical study data. Significant experience working with CDISC and related FDA standards for specification and creation of SDTM and ...

Therapeutics Inc

Sr. Biostatistician

San Diego, CA

Write and/or supervise SAS programming and QC to create SDTM and ADaM data sets, tables, figures and listings for clinical study reports (CSRs). * Perform statistical analyses of data and interpret ...

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How much do sdtm programmer jobs pay per hour?

As of Aug 18, 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.

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.

What are the most commonly searched types of Sdtm Programmer jobs in California?

The most popular types of Sdtm Programmer jobs in California are:

What are popular job titles related to Sdtm Programmer jobs in California?

For Sdtm Programmer jobs in California, the most frequently searched job titles are:

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Sdtm Programmer jobs near you
Infographic showing various Sdtm Programmer job openings in California as of August 2026, with employment types broken down into 78% Full Time, and 22% Contract. Highlights an 74% In-person, and 26% Remote job distribution, with an average salary of $81,158 per year, or $39 per hour.

Associate Director, Statistical Programming

Revolution Medicines

Redwood City, CA • On-site

Full-time

Re-posted 6 days ago

Job description

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
The Opportunity:
Position requires 14+ years of Statistical Programming experience with exploratory-stage oncology clinical trials, providing programming support and oversight of one or more clinical programs (early or late phase) within Statistical Programming function. In addition to hands-on Programming, this position requires providing oversight and programming support and guidance for internal deliverables and regulatory submissions while ensuring conformance to CDISC standards and submission guidelines. Based on company needs, this position will be required to lead one or more early Phase or late phase studies/programs. Specific responsibilities include:
  • Effective collaborating with cross functional teams to provide programming timelines for various deliverables.
  • Provide SAS Programming technical support and guidance to programming team.
  • Oversight/participation in any internal/mock or regulatory authority audits.
  • Timeline and vendor management for deliverables, including submission-related activities, complying with regulatory standards (e.g., FDA 21 CFR Part 11, GxP).
  • Oversee the programming support for relevant deliverables, such as Investigator Brochures, publications, US and ex-US regulatory submissions, including CDISC compliant datasets (SDTM, ADaM) and data documentation, Reviewer's Guide, TLFs, Statistical Analysis Plans (study specific, ISS, ISE, Exposure-Response), blank and annotated CRFs, and actual patient CRFs.
  • Hands-on programming and management of in-house deliverables including but not limited to Dose Committee meetings, Board of Director meetings, Exploratory Analysis, etc.
  • Oversight and Verification Review of documents, spreadsheets, slides for in-house presentations and external publications.

Titles may vary based on candidate experience.
Required Skills, Experience and Education:
  • 14+ years of Statistical Programming experience with early or late phase oncology trial studies.
  • BS/BA degree or other suitable qualification with relevance to the field.
  • Experience leading one or more statistical programming contractors, and programming vendors.
  • Proficiency in providing hands-on SAS Programming support for production or validation of analysis datasets, tables, listings and figures.
  • Demonstrated ability to multi-task, prioritize options, anticipate challenges, and execute goals as a member of an interdisciplinary team is extremely important.

Preferred Skills:
  • A demonstrable record of strong leadership and teamwork.
  • Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high energy environment.
  • Experience working in a small to mid sized biotech/pharma environment.
  • Experience collaborating on development of processes, SOPs and guidance documents for the Statistical Programming function.
    #LI-Hybrid #LI-DN1

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.
Base Pay Salary Range
$186,000-$233,000 USD
We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.
Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.
If you believe you've been contacted by someone impersonating a Revolution Medicines recruiter, please report it to careers@revmed.com so we can share these impersonations with our IT team for tracking and awareness.

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