- Lilly (Indianapolis, IN)
- … strategy, cross-functional priorities, and external engagement objectives + Lead in scientific point of view (POV) content creation for molecules beginning ... scientific channels. + Leverage emerging technologies, including AI-driven content solutions-to enhance message delivery and engagement with healthcare… more
- Lilly (Indianapolis, IN)
- …including thought leaders; and various medical activities in support of demand realization. The Sr . Director serves as a scientific resource for study teams, ... advisory boards, etc., and overseeing the development of the scientific content of educational programs). These responsibilities...trials (for example, phase I and II trials). The Senior Director is responsible for the planning,… more
- Lilly (Indianapolis, IN)
- …make life better for people around the world. **Purpose:** The purpose of the Senior Director Global Regulatory Affairs, Global Regulatory Lead (GRL) role is to ... of the regional regulatory scientists. **Primary Responsibilities:** **Regulatory and Scientific Expertise** _Develop,_ _Update and Execute_ _the Global Regulatory_… more
- Lilly (Indianapolis, IN)
- …Immunology team, and we are looking to add new experience and additional scientific capabilities to our team. This role will contribute to discovery- and ... skills, and experience presenting in large forums. + Experience with high- content data and familiarity with computational methodologies and artificial intelligence… more
- Lilly (Indianapolis, IN)
- …**Clinical Research/Trial/ Execution and Support** + Plans, collaborates on and reviews scientific content of clinical documents such as protocols, informed ... + Review lIT proposals and publications, as requested by CRP or Director -Medical. ** Scientific Data Dissemination/Exchange** + Knowledge of and compliance with… more
- Lilly (Indianapolis, IN)
- …make life better for people around the world. **Purpose:** The purpose of the Senior Director , Global Regulatory Affairs, Global Regulatory Lead (GRL) role is to ... experts as needed to inform development and manage issues. **Regulatory and Scientific Expertise** + Develop, Update and Implement the Global Regulatory Strategy -… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …studies align with strategic objectives of ICEPs. This position reports to the Senior Director , Global Integrated Evidence & Innovation Operations and can be ... **Summary:** The Global Integrated Evidence Operations, Associate Director role primarily focuses on leading and logistical management of integrated communication &… more
- Sumitomo Pharma (Indianapolis, IN)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Director Regulatory Affairs** . The Director is part of the Global ... clinical protocols/study reports, investigator brochures, CMC information/data) and contributes to content as needed + Advises team members of major regulatory… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. **Position Summary:** The Senior Director , Clinical Development will lead clinical development program(s) in ... for and ownership of design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports,… more
- Lilly (Indianapolis, IN)
- …Clinical Research/Trial Execution and Support + Plans, collaborates on and reviews scientific content of clinical documents such as protocols, informed consent ... and procedures. + Review IIT proposals and publications, as requested by Director -Medical. Scientific Data Dissemination/Exchange + Knowledge of and compliance… more