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Sr R & SAS Programmer
Job in
Chesterbrook, Chester County, Pennsylvania, USA
Listed on 2026-06-26
Listing for:
Atorus
Full Time
position Listed on 2026-06-26
Job specializations:
-
IT/Tech
Data Analyst, Data Scientist
Job Description & How to Apply Below
Sr SAS & R Programmer
Onsite in the Chesterbrook, PA area 3 days/week
SummaryThe 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 programming 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.
- 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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