- 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)
- …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
- Sumitomo Pharma (Indianapolis, IN)
- …dynamic, highly motivated, and experienced individual for the position of **Associate Director , Regulatory Affairs (Oncology).** The Associate Director is part ... clinical protocols/study reports, investigator brochures, CMC information/data) and contributes to content as needed + Advises team members of potential regulatory… 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
- Fujifilm (Indianapolis, IN)
- … scientific writing and presentation skills. You have the ability totranslate scientific and technical content into concise and persuasive market messages and ... **Position Overview** The Senior Product Marketing Manager, Viral Gene Therapy is a global role requiring proven experience in marketing strategy, demand generation,… 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