- 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
- Cytel (Boise, ID)
- …be a part of this new program. **Position Overview:** As a Senior Statistical Programmer , you will leverage your advanced SAS programming skills and proficiency ... lead one or more Early or Late stage clinical trials. **This role is Hybrid office based in...Science, Mathematics, etc. + At least 8 years of SAS programming working with clinical trial data… more
- Cytel (Cambridge, MA)
- …be a part of this new program. **Position Overview:** As a Senior Statistical Programmer , you will leverage your advanced SAS programming skills and proficiency ... in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical ...Science, Mathematics, etc. + At least 8 years of SAS programming working with clinical trial data… 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
- Regeneron Pharmaceuticals (Warren, NJ)
- JOB RESPONSIBILITIES: * Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data ... timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and...in the biotechnology, pharmaceutical or health related industry. * SAS Certification desirable. EXPERIENCE: * 3 - 5 Year… more
- IQVIA (Durham, NC)
- **Principal Statistical Programmer ** **Location** : home-based anywhere in the United States or Canada **Why IQVIA** Data Sciences Staffing Solutions, DSSS or DS3, ... and supported pooling of PK parameters required + Strong SAS technical skills and in-depth CDISC knowledge + Good...has worked in-depth with PKPD/Phase 1 studies. + Project/Study lead experience strongly preferred but not required . IQVIA… 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
- 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