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Senior Sdtm Programmer Jobs (NOW HIRING)

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 ...

IQVIA

Senior Statistical Programmer

Durham, NC · On-site +1

$139K - $165K/yr

Senior Statistical Programmer, IQVIA RDS Inc. Durham, NC. May telecommute (work from home) from ... SDTM) and Analysis Data Model (ADaM) datasets. Produce and validate statistical outputs such as ...

IQVIA, Inc.

Senior Statistical Programmer

Durham, NC · On-site

$139K - $165K/yr

Senior Statistical Programmer, IQVIA RDS Inc. Durham, NC. May telecommute (work from home) from ... SDTM) and Analysis Data Model (ADaM) datasets. Produce and validate statistical outputs such as ...

Recor Medical

Senior Clinical Programmer

Palo Alto, CA

$145K - $156K/yr

Position Summary The Senior Clinical Programmer at ReCor Medical requires complete knowledge and ... Establish and enforce data standardization practices (e.g., CDISC, SDTM, ADaM) * Collaborate with ...

MSD

Senior Statistical Programmer

Rahway, NJ

The senior statistical programmer will gather and interpret user requirements for programming ... Experience in CDISC SDTM and ADaM standards * Significant SAS or R programming experience for data ...

MSD

Senior Statistical Programmer

North Wales, PA

The senior statistical programmer will gather and interpret user requirements for programming ... Experience in CDISC SDTM and ADaM standards * Significant SAS or R programming experience for data ...

Certara USA, Inc.

Senior SAS Developer

Wayne, PA · On-site

We are seeking a highly skilled Senior SAS developer to support Clinical Data Automation with ... Work with clinical trial datasets including SDTM, ADaM, Define.xml, Reviewer's Guides, and ...

EDETEK

Senior Statistical Programmer

Edetek is seeking a highly skilled Senior Statistical Programmer to join our dynamic team. As a ... Develop and validate SAS programs to generate SDTM, ADaM datasets, tables, listings, and figures ...

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Senior Sdtm Programmer information

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How much do senior sdtm programmer jobs pay per hour?

As of Jul 21, 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 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.

Sr R & SAS Programmer

Atorus Research

Chesterbrook, PA • On-site

Contractor

Re-posted 3 days ago

Job description

Sr SAS & R Programmer
onsite in the Chesterbrook, PA area 3 days/week
SUMMARY
The contract Senior Statistical Programmer is a member of the Biometrics Department within the Research and Development (R&D) organization who supports Statistical programming work in accordance with corporate standard operating procedures (SOPs), GCP, 21 CFR and ICH guidance.
RESPONSIBILITIES
Program and validate derived datasets, tables, figures, listings. Process data from the external sources.
Perform ad hoc exploratory analyses for publications and programming support other functions of Research and Development or other organizations.
Oversee programing work/deliverables from CROs.
Contribute to the design/implementation/review of Case Report Form, Data Transfer Specification, Statistical Analysis Plan, SDTM/ADaM Specification documents, Define packages.
Program and validate CDISC compliant deliveries for the electronic submissions.
Support in the creation of supporting documentation for submissions.
Ensure programming deliverables are on time and of high quality.
Help managing internal contractors and external vendors.
Participate in development of departmental working instructions and guidelines.
Help in creation of enhanced functions/macros and utilities.
REQUIREMENTS
Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related discipline.
BS with more than 5 or MS with 3 years of experience in statistical programming (SAS, R) in the pharmaceutical industry.
Working knowledge of SAS and its various components.
Knowledge of R programming in clinical trials
Familiarity of the drug development process.
Knowledge of CDISC standards and electronic submission requirements.
Strong SAS and SAS Macro language skills.
R programming skills in clinical trials
Strong knowledge of industry standards.
Ability to work on data integrations (ISS and ISE).
Strong oral and written communication skills. Ability to communicate details of the analysis to other team members with less technical experience.
Ability to manage the timeline well and work in multi-project environment.

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