- Astrix Technology (NJ)
- …Clinical Project Manager + Site Start Up Specialists + Clinical Data Manager + Clinical Development Associates + SAS Programmer + and more! We are an ... ** Clinical Operations Professionals** Clinical Remote, NJ, US + Added - 06/02/2025 Apply for Job Astrix has been partnered with the Life Sciences industries for… more
- University of Southern California (Los Angeles, CA)
- …excellence, and private and public sector engagement, is looking for a Senior SAS Research Programmer to provide programming support on research projects ... behavior research and related health policy topics. The Senior SAS Research Programmer will serve as lead...uniquely spans the entire spectrum of pharmaceutical development and clinical care - from drug discovery to regulatory approaches… more
- University of Miami (Miami, FL)
- …of Neurology has an exciting opportunity for a Full-time or Part-time statistical programmer to join an active clinical and translational research group focused ... ALS) in Miami, FL. Core Job Summary The statistical programmer will be an integral member of the research...checks to ensure data integrity and completeness + Write SAS macros and programs for data cleaning, reporting (eg… more
- Merck (Rahway, NJ)
- …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial environment + MS in ... Applied Mathematics, Life Sciences, Engineering or related field plus 3-7 years SAS programming experience in a clinical trial environment **Department Required… more
- Geisinger (Danville, PA)
- …needed to provide statistical support to clinical investigators. + Experienced SAS or R programmer for both data manipulation and statistical analysis. ... master's-level biostatistician. Responsibilities include collaborating on the design of clinical research studies, writing biostatistical analysis plans for research… more
- Merck (North Wales, PA)
- …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial environment + MS in ... Applied Mathematics, Life Sciences, Engineering or related field plus 3 years SAS programming experience in a clinical trial environment **Department Required… more
- Merck (North Wales, PA)
- …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial environment + MS in ... Life Sciences, Engineering or related field plus 3 years SAS programming experience in a clinical trial...3 years SAS programming experience in a clinical trial environment _Department Required Skills and Experience:_ +… more
- IQVIA (Durham, NC)
- …or related. + Proficient in data visualization software - Spotfire. + Demonstrates SAS programming proficiency. + Knowledge of clinical trial study design and ... work in a data visualization team, safety statistical programming. The statistical programmer works collaboratively with the end users, internal colleagues to ensure… more
- Regeneron Pharmaceuticals (Warren, NJ)
- A principal statistical programmer provides timely support to the study team on all programming matters according to the project strategies. **In this role, a ... project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a...for you if can:** * Support and/or lead programmer for programming and QC of analysis datasets, TFLs… more
- Merck (Rahway, NJ)
- …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
- Merck (North Wales, PA)
- …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial environment + MS in ... Applied Mathematics, Life Sciences, Engineering or related field plus 3-7 years SAS programming experience in a clinical trial environment **Department Required… more
- Merck (North Wales, PA)
- …Company Biostatistics and Research Decision Sciences (BARDS) group. The senior statistical programmer utilizes multiple programming languages including SAS and R ... risk factors, describe drug utilization patterns and disease progression, answer clinical development questions, and support regulatory submissions using Real World… more
- IQVIA (Durham, NC)
- …to development of protocols, analysis plans, PK/PD analysis, and pharmacometric reports for pre- clinical or Phase I-IV clinical studies. + Consult with ... Clinical Pharmacology staff on study design, analyses, clinical development plans. + Plan and execute a wide range of pharmacometric analyses to inform … more
- Ascendis Pharma (Palo Alto, CA)
- …at least 7 years of relevant experience. + Proven experience as a lead programmer for clinical trials and complex technical projects. + Excellent knowledge of ... will be expected to provide timely and strategic programming support to clinical study teams in alignment with project goals. This role combines hands-on… more
- Trinity Health (Livonia, MI)
- …accordance with national and professional society standards and support various clinical initiatives aligned with achievement of the triple aim. Develops analytical ... solutions. Provides analytic consultation in collaboration with other team members ( clinical leaders, project managers, other analysts, etc.) in identifying analytic… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …years of clinical trial experience as a statistician and/or statistical programmer in the pharmaceutical, biotech, or CRO industry + Experience in Phases I-III ... contribute to study design, protocol development, case report form development, clinical study reports, and exhibits for other reports and presentations.… more
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