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Senior Sdtm Programmer Jobs (NOW HIRING)

Immunome, Inc.

Senior EDC Programmer

Bothell, WA · On-site

$115K - $150K/yr

Position Overview The Senior EDC (Electronic Data Capture) Programmer (Sr. EDCP) is responsible for ... Collaborate with Data Management to ensure alignment with data standards (CDISC, SDTM where ...

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 ...

Immunome, Inc.

SeniorEDC Programmer

Bothell, WA

Position Overview The Senior EDC (Electronic Data Capture) Programmer (Sr. EDCP) is responsible for ... Collaborate with Data Management to ensure alignment with data standards (CDISC, SDTM where ...

Atorus Research

Sr R & SAS Programmer

Chesterbrook, PA · On-site

Sr SAS & R Programmer onsite in the Chesterbrook, PA area 3 days/week SUMMARY The contract Senior ... Plan, SDTM/ADaM Specification documents, Define packages. Program and validate CDISC compliant ...

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Senior Sdtm Programmer information

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How much do senior sdtm programmer jobs pay per hour?

As of Jun 9, 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 are Senior SDTM Programmers?

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.
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Senior Sdtm Programmer jobs near you
Infographic showing various Senior Sdtm Programmer job openings in the United States as of May 2026, with employment types broken down into 100% Contract. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $108,736 per year, or $52.3 per hour.
Senior Statistical Programmer - Remote

Senior Statistical Programmer - Remote

Penfield Search Partners

Fairfield, CT • On-site, Remote

Other

Posted 24 days ago

Job description

Job Description Contact: Neisha Camacho/Terra Parsons - teamnt@penfieldsearch.com No 3rd party candidates Senior Statistical Programmer to support programming activities within CNS in support of clinical trials and regulatory submissions. In this role, you will transform raw clinical data into analysis ready datasets, generate high-quality TLFs, and contribute to the continuous improvement of analysis workflows and programming processes. Key Responsibilities: Provide statistical programming support to generate SDTM and ADaM data sets, tables, listings, and figures for individual studies as well as ISS/ISE analyses

Provide programming support to internal teams including identifying, reporting, and resolving raw data issues Participate in the review of statistical analysis plans, table specification, develop specification for SDTM and ADaM data sets. Participate in study team meetings and address issues that may affect statistical programming. Support and participate in the preparation of clinical study reports, regulatory submissions, and annual DSUR and safety reports.

Perform ad hoc analyses and data validation. Develop and maintain necessary programming macros or tools to effectively support all programming needs Develop and contribute to internal teams SOPs and working documents related to EDC studies, FDA requests, independent validation, and general statistical programming processes. Qualifications Bachelor's or Master's degree in biostatistics, computer science, or related fields 8 years in statistical programming within the pharmaceutical, biotechnology, or CRO industry, including regulatory submissions within CNS is preferred.

Advanced SAS programming; CDISC standards expertise; knowledge of additional programming languages (R, Python) is a plus. Strong Macro and tool development and validation Experience in BLA, NDA/sNDA submissions. Proficiency in additional programming languages such as R or Python, along with experience using SAS/Graph and statistical packages, is preferred.

Strong communication skills and the ability to collaborate within cross-functional teams to manage priorities and meet deadlines are essential.

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