- 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
- Lilly (Indianapolis, IN)
- …for people who are determined to make life better for people around the world. The Clinical Study Build Programmer is responsible for programming and ... the mapping, testing and normalization of data into a clinical data warehouse. This requires an in-depth understanding of...MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to study build deliverables + Integrates multi-functional and/or… 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
- Cytel (St. Paul, MN)
- …+ At least 12 years progressive Clinical Research Experience + Medidata Rave Certified Study Builder + 10 years' experience as a database programmer + ... Experienced Medidata RAVE programmer to maintain Rave URL and be the...Maintain Core Configuration, ensuring consistency and efficiency across all studies + Maintain Cloud Admin EDC roles, ensuring consistency… more
- Sanofi Group (Morristown, NJ)
- …**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