ZipRecruiter

Log In

1

Senior Sdtm Programmer Jobs (NOW HIRING)

Navitas Life Sciences

Senior Statistical Programmer

The Senior Statistical Programmer Analyst I (SR SPA I) is an independent statistical programmer ... Critical client project activities are reporting database development (SDTM and ADaM), statistical ...

Cytel

Senior Statistical Programmer FSP

Cambridge, MA · On-site +1

As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical ... Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures ...

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 ...

Allucent

Senior Clinical Programmer I

We're looking for a Senior Clinical Programmer I who thrives on solving complex challenges and ... Champion industry standards and quality, applying CDISC conventions (CDASH, SDTM, TAUGs ...

next page

Showing results 1-20

All JobsSdtm Programmer JobsSenior Sdtm Programmer Jobs

Senior Sdtm Programmer information

See salary details

$13

$52

$71

How much do senior sdtm programmer jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for senior sdtm programmer in the United States is $52.28, according to ZipRecruiter salary data. Most workers in this role earn between $43.99 and $62.50 per hour, depending on experience, location, and employer.

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

AspectSenior Sdtm ProgrammerClinical Data Coordinator
CredentialsTypically requires a degree in life sciences or related field, with experience in SDTM programmingUsually holds a degree in health sciences, nursing, or related field, with data management training
Work EnvironmentWorks primarily in clinical trial data programming, using SAS or similar toolsManages data entry, cleaning, and validation in clinical trial settings
Industry UsageCommonly employed in pharmaceutical and biotech companies for SDTM data standardizationFound in clinical research organizations, hospitals, and pharmaceutical companies

The main difference is that Senior Sdtm Programmers focus on programming and data standardization using SDTM standards, while Clinical Data Coordinators handle data collection, entry, and quality control. Both roles are essential in clinical trials but differ in technical scope and responsibilities.

What are the typical collaboration points between a Senior SDTM Programmer and clinical data management teams?

As a Senior SDTM Programmer, you frequently collaborate with clinical data management teams to ensure data collected from clinical trials is accurately mapped and transformed into SDTM-compliant datasets. This often involves clarifying data specifications, resolving data discrepancies, and aligning on timelines for data delivery. Close communication helps maintain data integrity and compliance with regulatory standards, making teamwork and proactive problem-solving crucial aspects of the role.

What is a Senior SDTM Programmer?

Senior SDTM Programmers are experienced professionals in clinical data management who specialize in mapping and converting clinical trial data into the Study Data Tabulation Model (SDTM) format according to regulatory requirements. They ensure that data collected during clinical trials is structured, accurate, and compliant with standards set by organizations like the FDA and CDISC. Senior SDTM Programmers often lead programming activities, perform quality control checks, and collaborate with statisticians, data managers, and regulatory teams to prepare submission-ready datasets. Their expertise is vital for successful clinical trial submissions and regulatory approvals.

What are the key skills and qualifications needed to thrive as a Senior SDTM Programmer, and why are they important?

To excel as a Senior SDTM Programmer, you need deep expertise in clinical data standards (especially CDISC SDTM), advanced SAS programming skills, and a relevant degree in life sciences, statistics, or computer science. Familiarity with clinical trial data management systems, regulatory submission requirements, and tools like Pinnacle 21 are also crucial. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure data accuracy and smooth collaboration with cross-functional teams. These competencies are essential to deliver high-quality, regulatory-compliant datasets that support successful clinical trial submissions.
What cities are hiring for Senior Sdtm Programmer jobs? Cities with the most Senior Sdtm Programmer job openings:
What are the most commonly searched types of Sdtm Programmer jobs? The most popular types of Sdtm Programmer jobs are:
What states have the most Senior Sdtm Programmer jobs? States with the most job openings for Senior Sdtm Programmer jobs include:
Senior Sdtm Programmer jobs near you
Infographic showing various Senior Sdtm Programmer job openings in the United States as of July 2026, with employment types broken down into 85% Full Time, 6% Part Time, 1% Temporary, 6% Contract, 1% Nights, and 1% Summer. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $108,736 per year, or $52.3 per hour.

Senior Clinical Programmer - SDTM and R/SAS 3635027

Axiom Path

Bridgewater, NJ • Remote

$75 - $80/hr

Full-time

Posted 26 days ago

Job description

Be Part Of A High-Performing Team:

Join a growing clinical programming function within a science-driven biopharmaceutical organization developing therapies for patients with serious and rare diseases. This newly established team is bringing critical SDTM programming capabilities in-house and works closely with data management, biostatistics, and statistical programming. The environment is collaborative, technically rigorous, and well suited to an experienced programmer who enjoys building reliable clinical-data solutions while helping shape new internal processes.

What's In Store For You:

Engagement: W2 only (no C2C/1099)

This is a fully remote, 12-month consulting assignment open to candidates located anywhere in the United States. Availability during Eastern Time business hours is preferred.

The role offers the opportunity to become one of the early members of a growing clinical programming team and contribute directly to the organization’s transition from outsourced SDTM programming to an internal delivery model. A contract extension may be possible based on performance and business needs, although permanent conversion is not currently planned.

How You Will Make An Impact:

  • Create production-quality SDTM datasets using both SAS and R.
  • Independently perform quality control and validation of SDTM datasets.
  • Develop dataset specifications using CDISC standards and current SDTM Implementation Guides.
  • Create annotated CRFs, including domain mappings, annotation boxes, controlled terminology, and page-level placement.
  • Apply existing team macros and programming utilities to support annotated CRF and SDTM production.
  • Develop SAS- and R-based listings and reports supporting medical monitoring, clinical data management, and statistical endpoint monitoring.
  • Perform clinical-data checks, reconciliations, and issue investigation as assigned.
  • Collaborate closely with data managers, biostatisticians, statistical programmers, and clinical-study stakeholders.
  • Help establish scalable internal standards, workflows, and quality practices as SDTM programming transitions in-house.
  • Manage multiple study deliverables independently while maintaining accuracy, traceability, and timely execution.

Do you bring proven success in SDTM programming with both SAS and R?

  • Approximately 8–10 years of hands-on clinical programming experience in pharmaceutical, biotechnology, CRO, or related regulated clinical environments.
  • Strong production programming proficiency in both SAS and R.
  • Demonstrated experience creating and independently quality-checking SDTM datasets.
  • Strong knowledge of CDISC standards and current SDTM Implementation Guides.
  • Hands-on experience creating annotated CRFs, including page-level annotations and terminology mapping.
  • Ability to use established macros, functions, and programming utilities.
  • Experience translating raw clinical data, CRFs, specifications, and programming standards into compliant SDTM deliverables.
  • Strong analytical, troubleshooting, documentation, and quality-control skills.
  • Ability to work independently as an individual contributor in a small and evolving team.
  • Strong written and verbal communication skills.
  • Experience with JReview is highly preferred.
  • Experience with Shiny, Pharmaverse, or R Markdown is highly desirable.
  • Exposure to SQL programming is preferred.
  • Experience supporting medical monitoring, data-management reports, reconciliations, or statistical endpoint monitoring is beneficial.