- 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)
- …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)
- …thought leaders; and various medical activities in support of demand realization. The Senior /Executive Director serves as a scientific resource for study ... at conferences, advisory boards, etc., and overseeing the development of the scientific content of educational programs). These responsibilities are generally… more
- Lilly (Indianapolis, IN)
- …people who are determined to make life better for people around the world. The Senior Director of Gene Therapy Medical Affairs will work across our gene therapy ... about genetic testing and gene therapy. Develop and review medical and scientific content for presentations and provide education to internal teams and external… 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
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... guidance, Federal Register notices, public commenting opportunities, and newsletter content . + Manage development and distribution of weekly regulatory 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 consent ... and procedures. + Review IIT proposals and publications, as requested by Director -Medical. Scientific Data Dissemination/Exchange + Knowledge of and compliance… more