- Cytel (Trenton, NJ)
- …& R-Shiny. + At least 5 years of R/ SAS programming experience with clinical trial data . + General knowledge of regulatory requirements and drug development ... programmer will also be required to utilize the SAS software system; they should be proficient in ...support electronic regulatory submissions; providing systems and support for clinical data management staff, clinical … more
- Cytel (Trenton, NJ)
- …Performing data manipulation, analysis and reporting of clinical trial data , both safety and efficacy (ISS/ISE), utilizing SAS programming + Production ... this new program. **Position Overview:** As a Senior Statistical Programmer , you will leverage your advanced SAS ...8 years of SAS programming working with clinical trial data in the Pharmaceutical &… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …study, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to ... A principal statistical programmer provides timely support to the study team...with 3+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical… more
- Merck (Rahway, NJ)
- …Specific Required Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS /MACRO, ... Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial...understanding of statistical terminology and concepts. + Familiarity with clinical data management concepts + Experience in… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …or related discipline with 3+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related ... JOB RESPONSIBILITIES: * Support and/or lead programmer for programming and QC of analysis datasets,...analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements. Assist in the coordination… more
- Cytel (Trenton, NJ)
- …Clinical Development, and other functional representatives to develop, maintain and document clinical data standards. This role also acts as a statistical ... + Provides technical and/or operational guidance in the application of industry clinical data standards within the statistical programming data … more
- Astrix Technology (NJ)
- … Project Manager + Site Start Up Specialists + Clinical Data Manager + Clinical Development Associates + SAS Programmer + and more! We are an equal ... ** Clinical Operations Professionals** Clinical Remote, NJ, US Pay Rate Low: 25 | Pay Rate High: 80 + Added - 06/02/2025 Apply for Job Astrix has been partnered… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …training and ensure effective implementation of SDTM, ADaM and TLFs standard in clinical trial data analysis - Develop and maintain necessary programming macros ... for the programming technical decision. By guiding other internal programmer or by self, perform programmatic review of Study...- Advanced working knowledge of all aspects of the SAS programming language used in clinical trials… more
- Sanofi Group (Morristown, NJ)
- …**Main Responsibilities:** + Provide high quality input into the design of the clinical study (including protocol development), the setup and conduct of the study to ... make sure data are adequately captured and collected to answer the...quality control plan. + Perform and/or coordinate with study programmer the production of statistical analyses. Review and examine… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …you if have:** + Proficiency in SAS programming skills in a clinical data environment with excellent analytical skills. Knowledge of other programming ... The Manager Statistical Programmer will lead and support all programming activities...8+ (9+) years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical… more