- United Therapeutics (Research Triangle Park, NC)
- …and pulmonary diseases, and other orphan diseases. **How you'll contribute** The Clinical Data Management Programmer is responsible for both programming and ... for phase I - IV clinical & non- clinical trials. The CDM Programmer will create...IMPORT, EXPORT procedures and ODS OUTPUT + Experience using SAS within clinical trials (eg, DM or… more
- IQVIA (Nashville, TN)
- …complex project or client requirements. **Job Details:** + Position: - Principal Statistical Programmer + Home Based + Min 4+ 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
- Medical Mutual of Ohio (Brooklyn, OH)
- …design documentation processes. Lead Business Intelligence Programming Analyst The Lead Business Intelligence Programmer 's role will drive collaboration and ... Advantage, Medicare Supplement, and individual plans. The Business Intelligence Programmer Analyst is responsible for transforming business requirements into BI… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …teams on various clinical projects and may function as the Lead Clinical Data Programmer on multiple projects simultaneously. **Responsibilities** ... to support drug development processes and global submissions as required for clinical trials. These include developing and validating SAS programs for… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …the programming and project standard under minimal supervision of the lead programmer and manager to support ongoing clinical studies and requests for study ... Senior Statistical Programmer provides support to the lead programmer and study team on all...be for you if you have:** + Proficiency in SAS programming skills in a clinical data… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …**This role may be for you if have:** + Good SAS programming skills ( SAS (Base, Stat, Macro, graph) in a clinical data environment + Good understanding of ... A senior pharmacometrics programmer provides timely support to the study team...matters according to the project strategies. Processing/analyzing/storing data from clinical studies according to a Statistical Analysis Plan, … more
- Digital Prospectors (Bedford, MA)
- …and evolving environment. **Essential Duties and Responsibilities (but not limited to):** + Lead programming efforts for various clinical studies, from Phase 1 ... **Statistical Programmer ** **Bedford, MA** **Job Type:** Contract **Recruiter:** Hillary...provide programming support for Phase 1 through Phase 3 clinical trials, focusing on disease monitoring and project integration.… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Principal Statistical Programmer will lead and support all...may be for you if have:** + Proficiency in SAS programming skills in a clinical data ... to work independently implementing and driving the programming to support ongoing clinical studies and requests for study report, regulatory submission, and ad… more
- Dana-Farber Cancer Institute (Boston, MA)
- The Senior Data Programmer Analyst under the Associate Director, Data Analysis and Management, will be key to the completion of outcomes and translational research ... works closely with investigators, directors, program and project managers, clinical research coordinators, research data specialists, computational biologists and… more
- IQVIA (Durham, NC)
- … research setting. + Must have excellent knowledge of CDISC standards. + Strong SAS programming skills when applying to clinical trial data. + Moderate level ... **Summary:** IQVIA is hiring a Principal Statistical Programmer to join a sponsor-dedicated, RWE biometrics team....resource in this area. Apply your skills in both SAS and R programming. **Job Expectations:** + Serves as… more
- Harvard University (Cambridge, MA)
- …Administrator providing oversight for advanced application design and planning, Core programmer training, and clinical data standardization, respectively + ... applying: 1) Resume, 2) Cover letter, 3) Sample of SAS code (solely created by the applicant - preferably...seven years of high-level statistical programming skills in a clinical data environment or research setting, preferably with … more
- Amgen (Washington, DC)
- …the lives of patients while transforming your career. Biostatistical Programming Manager - Lead Developer **What you will do** Let's do this. Let's change the world. ... Global Statistical Programming (GSP) organization and the analysis and reporting of clinical trial data. We are actively making significant investments to modernize… more
- BeiGene (Emeryville, CA)
- …and assignment of programmers to ensure projects are appropriately staffed. + Lead or contribute to the development or adoption of departmental processes and ... providing guidance, coaching, and career development for all team members. + Lead or contribute to the selection and management of CROs (including strategic… more
- Amgen (Washington, DC)
- …required standards and are statistically accurate. The Biostatistical Programming Senior Manager (Product Lead Programmer ) lead a group of Oncology and other ... assigned staff at product level according to priorities. + Lead and/or participate in departmental process improvement initiatives and...industry experience **Preferred Qualifications:** + In depth knowledge of SAS Graph, SAS STAT, SAS … more
- Medtronic (Minneapolis, MN)
- …and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, ... design and analysis of scientific data including, but not limited to, clinical studies and research experiments. Represents Medtronic from a statistical perspective… more
- Sanofi Group (Cambridge, MA)
- …we have a shared commitment to bring innovation and rigor to oncology clinical development. As Associate Statistical Project Leader, you will lead several ... lives. **Major Duties and Responsibilities:** Provide support and leadership to the clinical trial study and/or project team on all relevant statistical matters: +… more
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