1

Day Sdtm Programmer Jobs (NOW HIRING)

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 ...

Electronic submission of clinical data to agencies, e.g. e-CTD guidance and CDISC SDTM and ADaM ... On-site in Boston (recommended 2-3 days hybrid) or 100% remote with occasional travel to Boston ...

Develop and validate SAS programs to generate SDTM, ADaM datasets, tables, listings, and figures ... Paid vacation time and sick days * Corporate holidays annually * Participation in the 401K Plan

next page

Showing results 1-20

Day Sdtm Programmer information

See salary details

$12

$39

$68

How much do day sdtm programmer jobs pay per hour?

As of Jun 24, 2026, the average hourly pay for day sdtm programmer in the United States is $39.54, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $51.44 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Sdtm Programmer jobs? The most popular types of Sdtm Programmer jobs are:

Sr R & SAS Programmer

Atorus Research

Chesterbrook, PA • On-site

Contractor

Posted 6 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.