- Merck & Co. (Rahway, NJ)
- …Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS /MACRO, ... and programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data , transform the … more
- Merck & Co. (North Wales, PA)
- …Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS /MACRO, ... be programmed, an understanding of statistical terminology and concepts.Familiarity with clinical data management conceptsExperience in CDISC and ADaM… more
- Merck & Co. (North Wales, PA)
- …Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS /MACRO, ... Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial...an understanding of statistical terminology and concepts Familiarity with clinical data management concepts Experience in CDISC… more
- Merck & Co. (Rahway, NJ)
- …and information into simple readable formSolid project management skillsFamiliarity with clinical data management conceptsStrategic thinking - ability to turn ... 10%Flexible Work Arrangements:HybridShift:Not IndicatedValid Driving License:NoHazardous Material(s):N/ARequired Skills:Business, Business, Clinical Data , Clinical Databases, … more
- Merck & Co. (Rahway, NJ)
- …experience in a clinical trial environment.Required Experience and SkillsMust possess SAS programming skills including data steps, procedures, SAS /MACRO, ... and reporting deliverables under the guidance of a senior-level programmer supporting early-phase oncology clinical trials. Collaborate... study reports, and new drug application filing. Produce SAS data transport files and program text… more
- Merck & Co. (Rahway, NJ)
- …Mathematics, Life Sciences, Engineering or related field plus at least 2 years SAS programming experience in a clinical trial environment. Required experience ... submission deliverables under the guidance of a senior level programmer .Perform validation tasks according to departmental SOPs and collaborate...and skills Must possess SAS programming skills including … more
- University of Southern California (Los Angeles, CA)
- …programmer and technical specialist on research projects that use administrative healthcare claims data . SAS is required. The programmer is an integral ... Senior SAS Research Programmer - USC Schaeffer CenterApply...programmer is to develop a plan to adapt data that are complex and very large in scope to… 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 ... support for the cleaning, summarizing/reporting, and analysis of research data . The statistical programmer will work most...+ Conduct routine data checks to ensure data integrity and completeness + Write SAS … more
- Insight Global (Minneapolis, MN)
- …is working with the extraction piece of the ETL process Using SAS to extract data Strong understanding of clinical / healthcare data to understand how to ... Skills and Requirements 5+ years of experience as an analyst- programmer performing various system development lifecycle functions 5+ years...SAS coding experience 5+ years of experience using SAS for data extraction from large volume… more
- J&J Family of Companies (Santa Clara, CA)
- …is a detail-oriented statistical programmer with a strong interest in clinical data analysis, regulatory processes (such as PMA or 510(k) submissions), ... review, and final study reports. + Collaborate with statisticians, data managers, clinical team members, and external...to posters, presentations, or ad hoc analyses, including visual data summaries using SAS graphics or other… more
- Cytel (Boise, ID)
- …Performing data manipulation, analysis and reporting of clinical trial data , both safety and efficacy (ISS/ISE), utilizing SAS programming + Production ... this new program. **Position Overview:** As a Senior Statistical Programmer , you will leverage your advanced SAS ...8 years of SAS programming working with clinical trial data in the Pharmaceutical &… more
- Cytel (Tallahassee, FL)
- …Performing data manipulation, analysis and reporting of clinical trial data , both safety and efficacy (ISS/ISE), utilizing SAS programming + Generating ... this new program. **Position Overview:** As a Senior Statistical Programmer , you will leverage your advanced SAS ...7 years of SAS programming working with clinical trial data in the Pharmaceutical &… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …study, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to ... A principal statistical programmer provides timely support to the study team...with 3+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical… more
- Merck (North Wales, PA)
- …Specific Required Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS /MACRO, ... Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial...understanding of statistical terminology and concepts + Familiarity with clinical data management concepts + Experience in… more
- Merck (North Wales, PA)
- …Specific Required Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS /MACRO, ... Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial...understanding of statistical terminology and concepts. + Familiarity with clinical data management concepts + Experience in… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …or related discipline with 3+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related ... JOB RESPONSIBILITIES: * Support and/or lead programmer for programming and QC of analysis datasets,...analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements. Assist in the coordination… 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 ... and supported pooling of PK parameters required + Strong SAS technical skills and in-depth CDISC knowledge + Good...experience working on Phase 1 studies specifically with PKPD data and having created ADPP and ADPC datasets **_required_**… more
- IQVIA (Washington, DC)
- …experience preferred. * SAS Certified preferred. * Strong knowledge of data standards for clinical research and statistical analysis including CDISC SDTM, ... programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and...ADaM, and ICH Statistical Principles for Clinical Trials. * Equivalent combination of education, training and… more
- Astrix Technology (NJ)
- … Project Manager + Site Start Up Specialists + Clinical Data Manager + Clinical Development Associates + SAS Programmer + and more! We are an equal ... ** Clinical Operations Professionals** Clinical Remote, NJ, US Pay Rate Low: 25 | Pay Rate High: 80 + Added - 06/02/2025 Apply for Job Astrix has been partnered… more
- Merck (Rahway, NJ)
- …requests, clinical study reports, and new drug application filing. Produce SAS data transport files and program text files for regulatory submission. ... analysis and reporting deliverables under the guidance of a senior-level programmer supporting early-phase oncology clinical trials. Collaborate with other… more
