- University of Miami (Miami, FL)
- …of Neurology has an exciting opportunity for a Full-time or Part-time statistical programmer to join an active clinical and translational research group focused ... support for the cleaning, summarizing/reporting, and analysis of research data . The statistical programmer will work most...+ Conduct routine data checks to ensure data integrity and completeness + Write SAS … more
- Cytel (Columbus, OH)
- …& 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
- Actalent (Durham, NC)
- Job Title: Analyst Programmer IIJob Description The Clinical Data Management Programmer II works under the supervision of the Clinical Data & ... maintain SAS programs and scripts to automate clinical data integration, cleaning, reshaping, and export...field. + 5+ years' experience with clinical data management. + 5+ years' experience with SAS… more
- Trinity Health (Syracuse, NY)
- …14 **Approved By:** Director of Business Intelligence & DSS **POSITION PURPOSE** The Data Programmer Analyst (I) serves as a technical resource to support ... decisions. Under the guidance of Senior Analysts, such as Data Scientists (Level II and Senior), Programmer ...Ability to learn and understand front-end source systems and clinical workflows for effective validation of data .… more
- Cytel (Columbus, OH)
- …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
- Actalent (Santa Monica, CA)
- …to detail. Work Environment The work environment includes frequent interaction with Clinical Data Science, Clinical Development, and Regulatory Affairs ... SAS (R)). The ideal candidate will successfully interact with Biometrics, Clinical Development, and Regulatory Affairs groups, perform data manipulation… more
- ThermoFisher Scientific (Bethesda, MD)
- …tables, and figures using SAS and standard tools. + Prepare and analyze clinical trial datasets (eg, lab data , vital signs, tumor response, imaging, quality ... through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development...and in the future! As part of GPHS, the Programmer Analyst/Sr. Programmer Analyst will engage in… 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
- AbbVie (North Chicago, IL)
- …Job Description Key Responsibilities + Create specifications for the structure of ADaM data sets for individual studies. + Develop SAS programs for creation ... guides & data definition documents. + Participate in development of SAS Macros. Qualifications Education & Experience Must possess a BS or foreign academic… more
- Merck (North Wales, PA)
- …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 5-9 years SAS programming experience in a clinical trial...understanding of statistical terminology and concepts + Familiarity with clinical data management concepts + Experience in… more
- Merck (North Wales, PA)
- …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 (Columbus, OH)
- …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
- Trinity Health (Livonia, MI)
- …and three to five (3-5) years of relevant operational, technical, healthcare or clinical data analytics experience; or an equivalent combination of education and ... data analyses through summarization, interpretation, and visualization of data so to make recommendations to clinical ...Office skills required, particularly in Excel. Proficient working with data in the capacity of a programmer .… more
- Teva Pharmaceuticals (West Chester, PA)
- …of experience in a pharmaceutical or clinical research setting as a programmer . **Compensation Data ** The annual starting salary for this position is between ... and new people to make a difference with. **The opportunity** The clinical programming department provides SAS programming support; develops and generates… 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
- BeiGene (San Mateo, CA)
- …industries or academic research. Experience with oncology trials. + Expert level SAS programmer with experience in delivering complex programming assignments and ... conducting statistical programming. + Oversee the work of staff in support of clinical trials, ad-hoc analysis requests, data validation, etc. in accordance with… 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
- Edwards Lifesciences (Sacramento, CA)
- …draft CRFs (Case Report Form), databases and perform edit checks + Partner with clinical data management team to ensure that the databases is defined consistency ... Develop, test, validate, document, maintain and execute programs in SAS and serve as lead programmer . He/she...in programming, documentation, validation and review of summary tables, data listings, and graphs for inclusion in clinical… more
- Edwards Lifesciences (Irvine, CA)
- …publications and podium presentations. + Create internal routine reports to support data cleaning, safety review, and clinical trial operation conduct. + ... Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical… more
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