- Merck (North Wales, PA)
- …data management concepts as applied to drug/vaccine development. + Expertise in applying SAS for clinical trial programming including data steps, procedures, ... global programming standards for efficacy analysis and reporting using R & SAS . + Develops and validates global programming standards for safety analysis and… more
- Terumo Neuro (Aliso Viejo, CA)
- …of a Clinical Data Manager, Clinical Quality Assurance Manager, and Clinical SAS Programmer team member as to how to plan and execute programming ... **12799BR** **Title:** Intern, Clinical Data Programmer and Clinical QA...majors. + Competent in at least one programming language ( SAS , R, or Python) + Fluency in using data… more
- Merck (North Wales, PA)
- …Applied Mathematics, Life Sciences, Engineering or related field plus at least 3 years SAS programming experience in a clinical trial environment. + **OR** a ... Engineering or related field plus at least 5 years SAS programming experience in a clinical trial...5 years SAS programming experience in a clinical trial environment. **Positions Required skills and expereince:** +… more
- Merck (North Wales, PA)
- …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. + MS in ... Engineering or related field plus 7 or more years SAS programming experience in a clinical trial...more years SAS programming experience in a clinical trial environment. **Department Required Skills and Experience:** +… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …International Conference on Harmonization (ICH) guidelines. The SA Manager will ensure the SAs provide clinical administrative support to the study teams and ... Associate Director, will supervise a group of Study Associates ( SAs ) or Senior SAs who assist in...who assist in planning and in the execution of clinical studies in adherence to the protocol, Good … more
- Boehringer Ingelheim (Ridgefield, CT)
- …Contract Research Organizations (CROs), regulatory authorities, or academic institutions; using SAS or R; applying understanding of clinical trial development ... SAS /BASE, SAS /MACRO, SAS /GRAPH, SAS /STAT, and SAS /SQL to map raw clinical data to CDISC-compliant datasets and create TFL for data monitoring, … more
- Cytel (Juneau, AK)
- …the clinical database; and building analysis databases composed of SAS datasets. The R/Shiny developer must follow established standardized design and ... code development & R-Shiny. + At least 5 years of R/ SAS programming experience with clinical trial data. + General knowledge of regulatory requirements and drug… more
- Bristol Myers Squibb (Tampa, FL)
- …analysis datasets and reports across all therapeutic areas. + Utilize expert knowledge of SAS or R to integrate clinical data and pharmacokinetic data to prepare ... more: careers.bms.com/working-with-us . **Position Summary** The Senior Data Scientist leverages SAS or R to integrate data from diverse sources for pharmacometric… more
- Cytel (Boston, MA)
- …following fields Statistics, Computer Science, Mathematics, etc. + At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & ... a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM...or lead one or more Early or Late stage clinical trials. **This role is Hybrid office based in… more
- University of Miami (Miami, FL)
- …for a Full-time or Part-time statistical programmer to join an active clinical and translational research group focused on therapy development for Lou Gehrig's ... checks to ensure data integrity and completeness + Write SAS macros and programs for data cleaning, reporting (eg...or a closely related analytical field + Experience in SAS programming + Excellent verbal and written communication skills… more
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