- Lilly (Indianapolis, IN)
- … Study Build Programmer - eCOA** is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and ... collaborate with Data and Analytics colleagues such as the Clinical Data Associate , Clinical Data...a deep understanding of the technology used to collect clinical trial data + Develops and tests… more
- Lilly (Indianapolis, IN)
- … Clinical Study Build Programmer is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and ... collaborate with Data and Analytics colleagues such as the Clinical Data Associate , Clinical Data...a deep understanding of the technology used to collect clinical trial data + Effectively apply knowledge… more
- Lilly (Indianapolis, IN)
- …internal and external data (eg, prevalence data, real world data and analytics, clinical trial enrollment data) analyses and insights to develop and advise ... world's greatest health challenges. **Purpose:** The purpose of the Associate Director Informaticist role is to support the design...asset profile, program strategy, and trial designs, while driving excellence and optimization, enabling more… more
- Lilly (Indianapolis, IN)
- …life-threatening condition who are unable or do not qualify to participate in a clinical trial and for whom no satisfactory alternative therapy is available. ... to make life better for people around the world. Associate , Externally Sponsored Research and Access Programs Drug Supply...for the global supply chain coordination of drug supply ( clinical trial supply in addition to Lilly… more
- Lilly (Indianapolis, IN)
- …the technical services, environmental monitoring and process microbiology groups within the Clinical Trial Bioprocess Pilot Plant, which is focused on producing ... instruments + Ensures GMP compliance of facilities, processes, and documentation in the Clinical Trial Bioprocess Pilot Plant and the organization remains in a… more
- Merck (Indianapolis, IN)
- …and retention efforts to achieve study milestones + Upon request from Global Clinical Trial Operations (GCTO), + Recommends study sites and identifies potential ... License:** Yes **Hazardous Material(s):** n/a **Required Skills:** Advisory Board Development, Clinical Engagement, Clinical Trial Support, Gastrointestinal… more
- Lilly (IN)
- …and effectively utilize for delivering the portfolio. + Collaborate with Clinical Operation Associate Director/Director to stimulate, collate, and facilitate ... The purpose of the job is to ensure ExploR&D has adequate Good Clinical Practices (GCP) systems in place that are properly executed. Responsibilities include… more
- Sumitomo Pharma (Indianapolis, IN)
- …marketed products. + Conduct safety surveillance over product life cycle, reviewing clinical trial and post-marketing Individual Case Safety Reports (ICSRs), ... highly motivated, and experienced individual for the position of ** Associate Medical Director.** The Associate Medical Director...safety of clinical trials, including monitoring of clinical trial safety and laboratory data. +… more
- Bristol Myers Squibb (Indianapolis, IN)
- …role, the Warehouse Associate shall provide tactile support of all clinical trial and future commercial receiving, material handling, shipping and ... for warehousing support related to domestic and international shipping and distribution of clinical trial and commercial products for RayzeBio programs. In this… more
- Lilly (Indianapolis, IN)
- …of Statistical Sciences, CDISC Standards, and/or Data Management with respect to clinical trial data collection, analysis and reporting activities + Effective ... to enable clinical development and speed medicines to patients. The Associate Director - Results Reporting Systems role requires broad expertise of the systems… more