- Biodata Partners, Inc. (Raleigh, NC)
- Job Title: Principal Clinical Programmer Job Code: CDM0016 Department Name: Clinical Data Management Reports to Title: Manager or above Job Summary: The ... Principal Clinical Programmer is a member of the...standard reporting and data visualization tools including JReview, and SAS tools. Knowledge of industry standard clinical … more
- 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
- IQVIA (Boston, MA)
- …complex project or client requirements. **Job Details:** + Position: - Principal Statistical Programmer + Home Based + Min 7+ years of CRO/Pharma Industry + ... Must have expertise of R programming as well as SAS (R) Base, and good knowledge of SAS (R)...+ Excellent application development skills. + Strong understanding of clinical trial data and extremely hands on in data… more
- Cytel (Tallahassee, FL)
- …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 7 years of SAS programming working with clinical trial data… 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
- Regeneron Pharmaceuticals (Basking Ridge, 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 (Basking Ridge, 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
- BeOne Medicines (Emeryville, CA)
- …industries or academic research. Experience with oncology trials. + Expert level SAS programmer with experience in delivering complex programming assignments and ... outputs for tables and graphs, validate statistical programs, write general SAS application codes, prepare documentation for electronic submissions, and explore new… more
- Edwards Lifesciences (Irvine, CA)
- …you'll make an impact:** + Develop, test, validate, document, maintain and execute programs in SAS and serve as lead programmer . + He/she will take primary ... expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of...role in review and validation of SAS programs created by more junior-level programmers. + Provide… 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
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Manager Statistical Programmer will lead and support all...may be for you if have:** + Proficiency in SAS programming skills in a clinical data ... quality. **In this role, a typical day might include the following:** Lead programming support within multiple studies/projects in various study activities to… 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
