- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other internal programmer or by self, perform programmatic review of Study Date Tabulation Model (SDTM) and analysis (including Analysis Data Model (ADaM)) ... Daiichi Sankyo programming efficiency by developing tools and macros and build up standard on SDTM/ADaM datasets, and TFLs.Responsibilities:- Supporting project lead… more
- Lilly (Indianapolis, IN)
- …for people who are determined to make life better for people around the world. The ** Clinical Study Build Programmer - eCOA** is responsible for ... technology, data flow, data standards, database programming, normalization and testing. The Clinical Study Build Programmer will collaborate with Data… more
- Cook Medical (West Lafayette, IN)
- …team of EDC Programmers to achieve global business needs. + Develop databases for clinical studies using approved EDC software systems. + Ensure compliance with ... process improvements, and training personnel to facilitate the EDC Programmer needs of global clinical projects. Responsibilities...mentorship role + Prior experience in the conduct of clinical studies , preferably in the medical device… more
- J&J Family of Companies (Santa Clara, CA)
- …programming templates, macros, and tools to ensure consistency, efficiency, and compliance across clinical studies . + Contribute to the creation and review of ... programs. The ideal candidate is a detail-oriented statistical programmer with a strong interest in clinical ...study reports. + Collaborate with statisticians, data managers, clinical team members, and external vendors to ensure timely… more
- Spurwink Services (Portland, ME)
- …technical skillset to join our growing IT Applications team as a Senior Programmer /Analyst. The ideal candidate will have a strong background or interest in project ... but not limited to Finance, Human Resource, Senior Leadership and Clinical Departments) to gather requirements, design, and develop front-end solutions that… more
- Sanofi Group (Cambridge, MA)
- …**Main Responsibilities:** + Provide high quality input into the design of the clinical study (including protocol development), the setup and conduct of the ... the quality control plan. + Perform and/or coordinate with study programmer the production of statistical analyses....into interpretation and discussion of results sections for the clinical study report (CSR) and/or publications to… more
- Sanofi Group (Bridgewater, NJ)
- …get started? **Main Responsibilities** + Provide high quality input into the design of the clinical study , the setup and conduct of the study + Accountable ... to the statistical analysis plan: perform and/or coordinate with study programmer the production of statistical analyses...into interpretation and discussion of results sections for the clinical study report and/or publications to ensure… more
- Edwards Lifesciences (Irvine, CA)
- …you'll make an impact:** + Lead statistical programming activities as a lead programmer for a study or projects, co-ordinate activities of supporting programmers ... your ideas and expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …other internal programmer or by self, perform programmatic review of Study Date Tabulation Model (SDTM) and analysis (including Analysis Data Model (ADaM)) ... Daiichi Sankyo programming efficiency by developing tools and macros and build up standard on SDTM/ADaM datasets, and TFLs. **Responsibilities:** - Supporting… more
