- University of Southern California (Los Angeles, CA)
- …health behavior research and related health policy topics. The Senior SAS Research Programmer will serve as lead programmer and technical specialist on ... Senior SAS Research Programmer - USC Schaeffer...Stata, SQL, Microsoft and Linux systems. + Serves as lead programmer or technical specialist on research… more
- J&J Family of Companies (Irvine, CA)
- …to wellness. Learn more at https://www.jnj.com/medtech We are currently recruiting for a Lead Statistical Programmer to join our team based in Irvine, CA. ... of analysis datasets, tables, listings, and graphs from assigned clinical sources using SAS and/or R; mentoring,...basic R programming is required + Demonstrated ability to lead teams to deliver critical milestones + Familiarity with… more
- J&J Family of Companies (Irvine, CA)
- …and generation of analysis datasets, tables, listings, and graphs from assigned clinical sources using SAS and/or R; leading development and maintenance ... Learn more at https://www.jnj.com/medtech We are currently recruiting for a Sr Statistical Programmer to join our team based in Irvine, CA. This role can be… more
- J&J Family of Companies (Titusville, NJ)
- …Johnson Innovative Medicine is searching for the best talent for the position of ** Clinical Programmer ** to join our Integrated Data Analytics and Reporting team ... have multiple openings for this position. Position Summary: The Clinical Programmer is an individual contributor with...reporting. May include SAS , R, Python, etc. SAS knowledge is preferred for Clinical Programming… more
- J&J Family of Companies (Irvine, CA)
- …Facilitate the delivery of standard metric reports. Design, implement, and maintain the SAS programming algorithm for the clinical study database and data ... America **Job Description:** **Employer:** Biosense Webster, Inc. **Job Title:** Senior Programmer **Job Code:** A011.6006 **Job Location:** Irvine, CA **Job Type:**… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …**A typical day as a Principal Programmer can include:** * Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools ... A principal statistical programmer provides timely support to the study team...project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a… more
- Johns Hopkins University (Baltimore, MD)
- …ACASI and/or Qualtrics. + Familiarity with a statistical analysis program (STATA, SAS or R preferred). Classified Title: Programmer Analyst Role/Level/Range: ... programming for projects with continued ongoing support. + Manage clinical and other types of data sets and conduct...processes and systems. + Ability to independently assess and lead others in which data management and statistical strategies… more
- IQVIA (Washington, DC)
- …and applications. * Fulfill project responsibilities at the level of statistical team lead for single complex studies or group of studies. * Understand the Scope ... field and 4 years relevant experience Req * Medical device experience preferred. * SAS Certified preferred. * Strong knowledge of data standards for clinical … more
- Teva Pharmaceuticals (West Chester, PA)
- …+ A minimum of 8 years of professional experience in a pharmaceutical or clinical research setting as a programmer including supporting regulatory submissions is ... Associate Director, Data Visualization & Analytics Projects Lead Date: Aug 26, 2025 Location: West Chester,...Hands-on expertise with R (Shiny, ggplot2), Python, Tableau/Spotfire and SAS is required. + Strong understanding of Clinical… more
- BeOne Medicines (San Mateo, CA)
- …industries or academic research. Experience with oncology trials. + Expert level SAS programmer with experience in delivering complex programming assignments and ... scientific subject, or equivalent related experience **Experience:** + Minimum 7+ years' clinical research and development programming experience using SAS + 2+… more
- Ascendis Pharma (Palo Alto, CA)
- …degree with at least 7 years of relevant experience. + Proven experience as a lead programmer for clinical trials and complex technical projects. + Excellent ... The successful candidate will serve as the Statistical Programming Lead for one or more clinical trials,...drug development process and regulatory requirements. + Proficiency in SAS programming, including the ability to develop and validate… more
- Sanofi Group (Cambridge, MA)
- …progress. Join our Biostatistics Neurology team as Associate Statistical Project Leader and you'll lead one or several late phase studies, or lead an indication ... Provide high quality input into the design of the clinical study, the setup and conduct of the study...the statistical analysis plan: perform and/or coordinate with study programmer the production of statistical analyses + Prepare statistical… more
- Sanofi Group (Cambridge, MA)
- …Immunology & Inflammation (I&I) as Associate Statistical Project Leader** and you will lead several I&I phase 2 or 3 studies under minimum supervision of statistical ... **Main Responsibilities:** + Provide high quality input into the design of the clinical study (including protocol development), the setup and conduct of the study to… more
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