- Merck & Co. (North Wales, PA)
- …and 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 reporting… more
- Merck & Co. (North Wales, PA)
- …Applied Mathematics, Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial environmentMS in Computer ... Life Sciences, Engineering or related field plus 3-7 years SAS programming experience in a clinical trial...3-7 years SAS programming experience in a clinical trial environment Department Required Skills and Experience: Effective… more
- Merck & Co. (North Wales, PA)
- …Mathematics, Life Sciences, Engineering or related field plus at least 3 years SAS programming experience in a clinical trial environment.OR a bachelor's degree ... 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:Must have experience… more
- Merck & Co. (North Wales, PA)
- …Applied Mathematics, Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer ... 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: Excellent… more
- Daiichi Sankyo, Inc. (Bernards, 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
- Genmab (NJ)
- …3-5 years of experience within the pharmaceutical industryHas experience with the SAS software packageAs Programming Manager, Clinical Programming, it is ... fit? Then we would love to have you join us!The Programming Manager, Clinical Programming is responsible for ensuring integrity, consistency and adherence to Study… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …utility development preferred- Advanced working knowledge of all aspects of the SAS programming language used in clinical trials programming preferred- Advanced ... to support submission QAs, perform ad-hoc and exploratory analysis requested by clinical team, and support agency response or potential Advisory Committee Meeting-… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …with a PhD preferred- Advanced working knowledge of all aspects of the SAS programming language used in clinical trials programming. preferred- Advanced working ... training and ensure implementation of ADaM and TLFs standard in clinical trials analysis- Provide programming support to prepare regulatory requested analyses… more
- Merck & Co. (Rahway, NJ)
- …writing detailed documentation, reviewing, running, and validating analyses in SAS , R, and SQL.Propose innovation study methodologies,data sources, and process ... study.Develop Reusable Code:-Efficiently develop and implement reusable analytics code in SAS , R, SQL for analyzing large databases, and provide clear documentation… more
- Merck & Co. (Boston, MA)
- …and analysis plansAccountable for reviewing and validating RWE analyses in SAS , R, and SQL executed by programming teamsExplore the suitability, completeness, ... statistics, biostatistics, econometrics, data science, biomedical informatics, health informatics, clinical informatics, epidemiology, health economics, biometrics, operations research, engineering,… more
- Aequor (South San Francisco, CA)
- …Analytics Leader The Position: The Data Analytics Leader (DAL) in gRED Early Clinical Development (ECD) Data Intelligence team supports ECD study teams by delivering ... and interpret data. The DAL works directly with ECD Clinical disease area leads, study team Clinical ...experience in creating SDTM, ADaM, and developing TFL using SAS or R/RShiny. 2&plus years of experience in RBQM… more
- Formation Bio (New York, NY)
- …than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of ... processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma… more
- Tris Pharma (Monmouth Junction, NJ)
- …statistical expertise and leadership in the design, analysis, and interpretation of clinical trials and other health-related research. The incumbent plays a crucial ... regulatory submissions. Provides expert statistical input in design and analysis of clinical trials and other research studies; Develops, reviews and provides input… more
- Genmab (NJ)
- …functions including Data Management, Statistics, Drug Safety, Medical, Clinical Pharmacology,Translational Research, Medical Writing, Project management, and ... and ADaM database standards. Supports specification and pooling of data across clinical trials within the same project. Supports submissions by ensuring that the… more
- 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
- 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 5-9 years SAS programming experience in a clinical trial environment + MS in ... Life Sciences, Engineering or related field plus 3-7 years SAS programming experience in a clinical trial...3-7 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 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
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