- IQVIA (Boston, MA)
- …database components and theory. + Excellent application development skills. + Strong understanding of clinical trial data and extremely hands on in data ... client requirements. **Job Details:** + Position: - Principal Statistical Programmer + Home Based + Min 7+ years of...ICH E6, ICH E3, ICH E8, ICH E9 and clinical research processes. + Minimum of 7+ years of… more
- J&J Family of Companies (Irvine, CA)
- …provide input on reporting processes and standards; + Support programming deliverables for clinical trials and support for any custom Data Management reports; + ... impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Data Analytics & Computational Sciences **Job Sub** **Function:** Biostatistics **Job… 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 ... + Strong, recent experience working on Phase 1 studies specifically with PKPD data and having created ADPP and ADPC datasets **_required_** + Hands-on experience… more
- Merck (Rahway, NJ)
- …be programmed, an understanding of statistical terminology and concepts. + Familiarity with clinical data management concepts + Experience in CDISC and ADaM ... Specific Required Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
- Merck (North Wales, PA)
- …be programmed; an understanding of statistical terminology and concepts + Familiarity with clinical data management concepts + Experience in CDISC and ADaM ... Specific Required Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
- IQVIA (Washington, DC)
- …device experience preferred. * SAS Certified preferred. * Strong knowledge of data standards for clinical research and statistical analysis including CDISC ... programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and...SDTM, ADaM, and ICH Statistical Principles for Clinical Trials. * Equivalent combination of education, training and… more
- Actalent (Seattle, WA)
- …standards. * Prior experience in the analysis of oncology and/or immunotherapy clinical trial data . KNOWLEDGE, SKILLS AND ABILITIES: * Effective communication ... fields). * A minimum of 5 years within the pharmaceutical, biotechnology or clinical research industry. * Proven experience using statistical software such as SAS, R… more
- Astrix Technology (NJ)
- …Manager + Site Start Up Specialists + Clinical Data Manager + Clinical Development Associates + SAS Programmer + and more! We are an equal opportunity ... ** 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)
- …analysis and reporting deliverables under the guidance of a senior-level programmer supporting early-phase oncology clinical trials. Collaborate with other ... and/or epidemiologists within BARDS, as well as stakeholders in data management, medical writing, and clinical operations...complete programming tasks under the guidance of a senior programmer at a project level; and to collaborate with… more
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