- 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
- 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
- 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 (Morristown, NJ)
- …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