- Lilly (Indianapolis, IN)
- …people around the world. Purpose: Trial Management Systems as part of Clinical Trial Foundations (CTF), within Clinical Design, Delivery and Analytics ... to patients. The Associate Director CTF Product Owner in Trial Management Systems will support operational and...development to drive the implementation of robust functionality within clinical systems to manage trial activities and… more
- Lilly (Indianapolis, IN)
- …following: clinical research, distribution, supply chain, logistics, clinical trial materials, project management, or direct quality support for any of ... organization is responsible for strategically planning and supplying materials, trial support services and innovative capabilities to... support services and innovative capabilities to support the execution of clinical trials globally… more
- Lilly (Indianapolis, IN)
- … process. **Scope -** Understand the scope of work required to complete the clinical trial successfully. Monitor the status and make adjustments and changes (per ... ( Clinical Research Organization) clinical development point of contact ** Clinical Trial Process Leadership and Expertise** Leverage and demonstrate broad… more
- Lilly (Indianapolis, IN)
- …to craft viable clinical scenarios. You will work to deliver complete clinical trial packages that enable rapid transition into trial execution. ... development of the asset strategy and translate to the clinical plan across Clinical Trial ...disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks… more
- Lilly (IN)
- …(CCSI) organization is responsible for strategically planning and supplying materials, trial support services and innovative capabilities to support ... devices. This role will also be responsible for vendor management to support the capabilities. **Responsibilities** Central Clinical Services + Ensure vendors… more
- Lilly (Indianapolis, IN)
- …product development activities over the entire spectrum of drug development and clinical trial phases. Specific activities include developing or contributing to ... of phase 3b/4 studies **,** as well as non clinical trial solutions/activities that are conducted in...disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks… more
- Lilly (Indianapolis, IN)
- …be accountable for compliance of team members. + Lead completion of clinical trial documents including protocols, amendments, investigator brochures, informed ... input for site selection, investigator meetings, steering committees, and clinical trial training. + Participate in data...disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks… more
- Lilly (Indianapolis, IN)
- … studies and trials. The successful candidate will collaborate cross-functionally to support clinical programs and pipeline programs as needed and will ... targets and goals + Collaborate with cross-functional teams to support clinical programs and achieve organizational and...history, and registry trials / studies) + Supports the clinical operations team, including clinical trial… more
- Lilly (Indianapolis, IN)
- …(CCSI) organization is responsible for strategically planning and supplying materials, trial support services and innovative capabilities to support ... protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members… more
- Lilly (Indianapolis, IN)
- … Study Build Programmer - eCOA** is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and ... a deep understanding of the technology used to collect clinical trial data + Develops and tests...disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks… more