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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 ...

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 ...

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 ...

Actalent

Senior Statistical Programmer

Princeton, NJ · Hybrid

$70 - $80/hr

Senior Statistical Programmer The Senior Statistical Programmer will provide comprehensive ... Oversee programming tasks, including SDTM, ADaM, and TLF preparation performed by vendors, while ...

Fortrea

Senior Programmer Analyst- Remote, US

$90K - $120K/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- Remote, US

$90K - $120K/yr

... programming or Visual Analytics tools like Spotfire or Tableau ... Develop/validate Custom/Complex SAS / SDTM datasets and efficiently handle external data and ...

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How much do senior sdtm programmer jobs pay per hour?

As of Aug 31, 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 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 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 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 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 cities are hiring for Senior Sdtm Programmer jobs?

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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 Statistical Programmer

Remote

Navitas Life Sciences
Scientific Research and Development Services • 501 - 1,000 employees
Learn more about Navitas Life Sciencesexternal

Full-time

Re-posted 25 days ago

Job description

Job Description
The Senior Statistical Programmer Analyst I (SR SPA I) is an independent statistical programmer analyst supporting the clinical reporting production programming and verification for client regulatory submissions and publications.
Critical client project activities are reporting database development (SDTM and ADaM), statistical and clinical reporting, verification and submissions support.
About the Role
  • Independently, perform SAS programming and analysis support of the generation of analysis datasets, statistical analysis, listings, figures and tables;
  • Independently, develop SAS application code;
  • Independently, perform validation of SAS programs and deliverables;
  • Independently, perform migrations and verifications;
  • Independently, perform SDTM and ADaM mapping;
  • Generate SDTM and ADaM deliverables;
  • Generate all necessary output for the compilation of statistical appendices for CTR, ISS, and ISE;
  • Generate data files and/or output for safety updates, publications and meeting presentations;
  • Interface with a cross-function of client and DataCeutics team members; and
  • Act as an Expert in one or more areas that may include Project Management, SCE, SDTM, ADaM, define.xml, SAS programming, deliverables process, Tables, Graphics, PK/PD, Registries or other areas.

Desirable Skills and Experience
  • Background in statistics and statistical analysis is desirable
  • 10 plus years Pharmaceutical or CRO industry experience in clinical reporting and statistical programming
  • Strong competence in SAS/Base, SAS/Macro, and SAS/STAT programming
  • Working knowledge of CDISC, SDTM and ADaM
  • Expert knowledge of SAS-based statistical programming
  • Proficiency in SAS programming on multiple platforms and operating systems, e.g. Windows, UNIX, etc. is desirable

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