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Full Time Sdtm Programmer Jobs (NOW HIRING)

Systimmune

Clinical Data Analyst, Spotfire

Redmond, WA · On-site

$90K - $130K/yr

This position requires a full-time onsite presence at our Redmond, WA office. Responsibilities ... programming, and data manipulation. * Familiarity with clinical trial data standards (CDISC SDTM ...

Genmab A/S

$186.88K - $280.32K/yr

Skilled SAS programmer with strong knowledge of CDISC SDTM/ADaM models, efficient coding practices ... Within the first year, regular full-time U.S. employees are eligible for: * 401(k) Plan: 100% match ...

Genmab A/S

Senior Programming Manager

$128.08K - $192.12K/yr

Skilled SAS programmer with strong knowledge of CDISC SDTM/ADaM models, efficient coding practices ... Within the first year, regular full-time U.S. employees are eligible for: * 401(k) Plan: 100% match ...

BioNTech SE

Director, Biostatistics (Oncology)

Cambridge, MA · On-site

$168.10K - $268.70K/yr

New Jersey, US | full time | Job ID: 9895 About this Role: As Director Biostatistics (Oncology) you ... Provide guidance to Statistical Programmers on SDTM/ADaM and TLFs specifications development and ...

SystImmune, Inc

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

This role is full-time onsite in Redmond, WA. Please note that SystImmune plans to relocate to a ... SAS, Python, and R programming knowledge is a plus. * Familiarity with CDISC standards (CDASH, SDTM ...

Systimmune

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

This role is full-time onsite in Redmond, WA. Please note that SystImmune plans to relocate to a ... SAS, Python, and R programming knowledge is a plus. * Familiarity with CDISC standards (CDASH, SDTM ...

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How much do full time sdtm programmer jobs pay per hour?

As of May 30, 2026, the average hourly pay for full time sdtm programmer in the United States is $54.18, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $81.49 per hour, depending on experience, location, and employer.

Is SAS a good career choice?

A career as a full-time SDTM programmer often involves using SAS software for clinical data management and analysis. SAS skills are highly valued in the pharmaceutical and healthcare industries, offering strong job stability and competitive salaries. Proficiency in SAS, along with knowledge of clinical data standards like SDTM, enhances employability in this field.

What is the difference between Full Time Sdtm Programmer vs Clinical Data Coordinator?

AspectFull Time Sdtm ProgrammerClinical Data Coordinator
Primary RoleDesigns and develops SDTM datasets for clinical trialsManages and oversees data collection and entry in clinical studies
Required SkillsProgramming, SAS, SDTM standardsData management, database systems, regulatory compliance
Work EnvironmentPharmaceutical or CROs, clinical research teamsClinical sites, research organizations, data management teams
CertificationsSAS certifications, knowledge of CDISC standardsData management certifications, possibly SAS or clinical research certifications

The Full Time Sdtm Programmer focuses on creating standardized datasets for analysis, requiring programming skills and SDTM expertise. In contrast, a Clinical Data Coordinator manages data collection and quality control during trials. Both roles are vital in clinical research but differ in technical focus and responsibilities.

More about Full Time Sdtm Programmer jobs
What cities are hiring for Full Time Sdtm Programmer jobs? Cities with the most Full Time Sdtm Programmer job openings:
What are the most commonly searched types of Sdtm Programmer jobs? The most popular types of Sdtm Programmer jobs are:
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Full Time Sdtm Programmer jobs near you
Infographic showing various Full Time Sdtm Programmer job openings in the United States as of May 2026, with employment types broken down into 50% As Needed, and 50% Temporary. Highlights an 100% Physical job distribution, with an average salary of $112,695 per year, or $54.2 per hour.
Principal Statistical Analyst

Principal Statistical Analyst

Revolution Medicines

Redwood City, CA • On-site

Full-time

Posted 15 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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