• Sr . Research Analyst - SAS

    University of Miami (Miami, FL)
    …of Miami has an exciting opportunity for a full-time or part-time statistical programmer to join an active clinical and translational research group focused ... Gehrig's disease (amyotrophic lateral sclerosis, or ALS). 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
    University of Miami (04/17/24)
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  • Sr . Programmer Analyst…

    ThermoFisher Scientific (Greenville, NC)
    …Office **Job Description** Company Name: PPD Development, LP Position Title: Sr . Programmer Analyst (Bioinformatics) Location: 929 North Front Street, ... considerations of research projects. Work independently in a lead programmer role on select moderately complex studies, or may...and working with complex data systems; Windows office applications; SAS Macro; Clinical research and trials; and… more
    ThermoFisher Scientific (06/18/24)
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  • Sr . Programmer /Analyst (United…

    Allucent (Cary, NC)
    …and Simulation (CPMS) team at Allucent in either Europe or USA. As a Senior Programmer /Analyst you will lead data programming and visualization activities across ... across the globe. We are looking for an R programmer to join our global Clinical Pharmacology...3 years of experience in data programming experience in SAS or R including 2 years in drug development,… more
    Allucent (04/20/24)
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  • Clinical Data Programmer , Oncology…

    Ascendis Pharma (Palo Alto, CA)
    …for employees to grow and develop their skills. The Clinical Data Programmer will be responsible for performing SAS programming ( SAS /SQL program ... clinical data review and process efficiency. The Clinical Programmer will lead clinical ...analytical skills using BASE/ SAS , SAS /STAT, SAS MACROS + Strong knowledge of Oncology clinical more
    Ascendis Pharma (04/19/24)
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  • Senior Analyst- Programmer I

    WuXi AppTec (San Diego, CA)
    … programming activities from different aspects (programming aspect, statistical aspect and clinical trial aspect) to ensure SAS programming activities to ... several therapeutic areas + Create, manage, and maintain the SAS programming algorithm for the clinical study...maintain the SAS programming algorithm for the clinical study database and data analysis, and contribute to… more
    WuXi AppTec (06/18/24)
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  • Senior Stat Programmer , Data…

    IQVIA (Durham, NC)
    …Follow steps to set-up studies and generate visualizations through Spotfire. + Preprocessing clinical data using SAS . + Producing data visualizations using ... real time data review. Also, this job requires industry experience working with clinical trial data._ IQVIA is hiring to expand a sponsor-dedicated team, working… more
    IQVIA (05/09/24)
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  • Senior /Principal Statistical…

    IQVIA (New Haven, CT)
    …areas. We are seeking a highly skilled and motivated Principal Statistical Programmer with expertise in pharmacokinetics (PK) and pharmacodynamics (PD) to join our ... dynamic FSP team. Position Overview: As a Principal Statistical Programmer with a specialized focus on PK/PD, you will...pivotal role in the design, execution, and analysis of clinical trials to support the development of our promising… more
    IQVIA (05/30/24)
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  • Senior Statistical Programmer , Late…

    Merck (North Wales, PA)
    …Applied Mathematics, Life Sciences, Engineering or related field and at least 5 years SAS programming experience in a clinical trial environment or + MS in ... Engineering or related field and at least 3 years SAS programming experience in a clinical trial...3 years SAS programming experience in a clinical trial environment. **Required Skills:** + Effective interpersonal skills… more
    Merck (05/25/24)
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  • Programmer

    Harvard University (Cambridge, MA)
    …real world data. The candidate will join a core team comprised of another Senior Programmer and two Programmers. CAUSALab is seeking a full-time Programmer ... related field + Statistical programming experience in include R, SAS and SQL a strong preference + Experience with...design, research methodology + Understanding of the healthcare domain, clinical , epidemiology and/or genomic data is a plus +… more
    Harvard University (06/19/24)
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  • Senior Scientist, Statistical…

    Merck (Rahway, NJ)
    …or related also accepted. + Experience must include 3 years in the following: SAS programming in a clinical trial environment, including data steps, procedures, ... **Job Description** **Responsibilities:** + Support statistical programming activities for clinical development projects. + This may include leadership of...SAS /MACRO, SAS /GRAPH, SAS systems and database expertise; designing… more
    Merck (06/13/24)
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  • Principal Statistical Programmer

    IQVIA (Durham, NC)
    …with a Global Pharma company. We are now expanding this team by adding a Senior or Principal level Statistical Programmer . Expect to be dedicated to this ... client relationships. **Our expectations of you:** + 8 years or more in SAS programming for clinical trial data, working within a CRO or Sponsor environment. + 3… more
    IQVIA (04/30/24)
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  • Senior Manager-Data Science (Statistical…

    Novo Nordisk (Plainsboro, NJ)
    About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... Science, serving as a key contact point into the Clinical Data Science and Evidence (CDSE) Real World Evidence...Evidence (CDSE) Real World Evidence (RWE) team. Relationships The Senior Manager reports directly to a Senior more
    Novo Nordisk (06/21/24)
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  • Senior Statistical Programmer

    IQVIA (Durham, NC)
    …from previous experience and knowledge. + Uses internal macros or writes SAS (R) macros to automate study deliverables. + Statistical programmers work collaboratively ... with biomarkers + Ability to program in R and SAS proficiently and learn new programming languages is required....leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We… more
    IQVIA (05/30/24)
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  • Senior Statistical Programmer - FSP

    IQVIA (Durham, NC)
    …over design, and supported pooling of PK parameters required** **Strong SAS technical skills and in-depth CDISC knowledge** **Good knowledge regulatory requirements ... or related field, and 6+ years of hands-on experience in Drug Development or clinical trials.** **This position is remote based (within United States or Canada) and… more
    IQVIA (06/08/24)
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  • Senior Analyst/ Programmer II

    WuXi AppTec (San Diego, CA)
    …in leading the programming activities for submissions **Skills** + Excellent skills in SAS programming or clinical studies + Excellent clinical trial ... knowledge is preferred + Working knowledge of other software such as S-plus and WinNonlin is preferred + Excellent knowledge in industry standards, such as the ICH guidelines, CDISC data standards, 21 CFR Part 11, and FDA guidelines, is required + Excellent… more
    WuXi AppTec (05/11/24)
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  • Programmer Analyst II - Center…

    UT Health (Houston, TX)
    Programmer Analyst II - Center for Healthcare Data...health outcomes. In this position, you will work with senior staff to create the coding required to extract ... you come in. **We are looking for a Full-Time Programmer Analyst II to join the Center for Healthcare...**_Preferred:_** + Experience with SQL,statistical analysis programs such as SAS , R or STATA + Any programming language PL/SQL,… more
    UT Health (05/20/24)
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  • IT Solution Analyst IV CCL Programmer

    Banner Health (AZ)
    …required. Strong technical skills as appropriate for position (SQL/Ansi SQL, SAS , Tableau, Excel, clinical software applications, etc.). PREFERRED QUALIFICATIONS ... **Primary City/State:** Arizona, Arizona **Department Name:** IT Clinical Care-Corp **Work Shift:** Day **Job Category:** Information...and mentor junior members of the team. As a senior level analyst, your assigned work will often be… more
    Banner Health (06/01/24)
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  • Sr . Biostatistician (North America)

    Allucent (Cary, NC)
    …helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need ... across the globe. We are looking for a Sr . Biostatistician (SrBios) to join our A-team (hybrid*/remote). As a SrBiosat Allucent, you are responsible for supporting… more
    Allucent (05/16/24)
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  • Associate Statistical Project Leader ( Sr

    Sanofi Group (Cambridge, MA)
    …leader and/or team leader. + Provide high quality input into the design of the clinical study, the setup and conduct of the study + Accountable for all statistical ... according to the statistical analysis plan: perform and/or coordinate with study programmer the production of statistical analyses + Prepare statistical methods &… more
    Sanofi Group (05/13/24)
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  • Associate Director of Statistical Programming

    Harvard University (Cambridge, MA)
    …Administrator providing oversight for advanced application design and planning, Core programmer training, and clinical data standardization, respectively + ... 65841BRAuto req ID:65841BRJob Code:384359 Sys Prog/Analysis/Admin Sr Department Office Location:USA - MA - Boston...applying: 1) Resume, 2) Cover letter, 3) Sample of SAS code (solely created by the applicant - preferably… more
    Harvard University (05/08/24)
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