- Merck (North Wales, PA)
- …level **Position Specific Required Skills and Experience:** + Programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic data ... in CDISC SDTM and ADaM standards + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH + Designs… more
- Merck (North Wales, PA)
- …be programmed, an understanding of statistical terminology and concepts. + Familiarity with clinical data management concepts + Experience in CDISC and ADaM ... Specific Required Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
- Merck (North Wales, PA)
- …be programmed; an understanding of statistical terminology and concepts + Familiarity with clinical data management concepts + Experience in CDISC and ADaM ... Specific Required Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
- Teva Pharmaceuticals (West Chester, PA)
- …the design and delivery of scalable, user-friendly interactive visualization solutions for clinical data exploration (Safety, Efficacy and other clinical ... dashboards and exploratory analytics to provide insights into our clinical trial data and to support decision-making...8 years of professional experience in a pharmaceutical or clinical research setting as a programmer including… more
- Merck (North Wales, PA)
- …datasets, and develop tables and figures according to the modeling analysis plans. The programmer will take on a data stewardship leadership role and be ... the creation of modeling data from original data source(s) to final modeling dataset. The programmer...Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures,… more
- Teva Pharmaceuticals (West Chester, PA)
- …contingent staff, and vendors + Partner with cross-functional stakeholders (Statistics, Data Management, Clinical Development, Regulatory) to ensure alignment ... of 10 years of experience in a pharmaceutical or clinical research setting as a programmer . +...multi-disciplinary pivotal projects to improve operational processes related to Clinical Trials execution and Data Presentation. Provides… more
- Geisinger (Danville, PA)
- …statistical support to clinical investigators. + Experienced SAS or R programmer for both data manipulation and statistical analysis. + Detail-oriented with ... support throughout all stages of the research process-from proposal development to data analysis and interpretation. Core members offer expertise in: * Refining… more
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