- Lilly (Indianapolis, IN)
- …of clinical studies and trials in all scientific aspects (eg, scientific advisory committees, data safety monitoring boards, medical monitoring) + Reviews ... for people around the world. **Role Overview** The Sr. Director , Clinical Development is an experienced clinical trialist who...trialist who will be responsible for the clinical and scientific execution of global clinical programs. They will play… more
- Lilly (IN)
- …are committed to continuing to build our leadership in it. As Associate Director , External Innovation Cardiovascular & Women's Health, this role will help develop ... preparation of in-depth documents clearly delineating the opportunity from a scientific and business perspective and partner interactions as projects progress from… more
- Lilly (Indianapolis, IN)
- …better for people around the world. **Purpose:** The purpose of the Senior Director Global Regulatory Affairs, Global Regulatory Lead (GRL) role is to develop and ... of the regional regulatory scientists. **Primary Responsibilities:** **Regulatory and Scientific Expertise** _Develop, Update and Execute the Global Regulatory… more
- Lilly (Indianapolis, IN)
- …life better for people around the world. **Purpose:** The Case Management Medical Review Scientist is responsible for conducting comprehensive medical review ... responsibilities and any related duties that might be required for the role/position. Medical review of ICSRs + Conduct comprehensive ICSR medical reviews across… more
- Lilly (Indianapolis, IN)
- …of ADCs, we are seeking a highly experienced and strategic Senior Director to lead our payload linker development efforts within the Antibody-Drug Conjugate ... payload linker process development. + Stay current of emerging technologies and scientific advancements in ADC linker and payload chemistry to maintain competitive… more
- Lilly (Indianapolis, IN)
- …better for people around the world. #WeAreLilly **Responsibilities:** The Associate Director - Quality Assurance (QA) API External Manufacturing is responsible for ... of externally manufactured small molecule (SM) APIs and Intermediates. The Assoc. Director QA must balance coaching the QA staff, prioritization and staffing for… more
- Lilly (Indianapolis, IN)
- …better for people around the world. **Purpose:** The purpose of the Senior Director , Global Regulatory Affairs, Global Regulatory Lead (GRL) role is to develop and ... experts as needed to inform development and manage issues. **Regulatory and Scientific Expertise** + Develop, Update and Implement the Global Regulatory Strategy -… more
- Lilly (Indianapolis, IN)
- …a track record of delivering impactful medicines that improve people's lives. ** Scientific and research leadership** + Provide strategic vision and direction for ... and next generation approaches to therapeutics. + Stay current with scientific literature, technology advancements, and external competitor progress to ensure the… more
- Lilly (Indianapolis, IN)
- …Large Molecule and Peptide APIs at external manufacturing facilities globally. The Sr. Director - Quality - Small Molecule API EM is the Site Quality Leader ... improvement to adapt to the business requirements. The Sr. Director - Quality - Small Molecule API EM is...Agreements. **Basic Requirements:** + BS or equivalent in a scientific field or engineering. + At least 10 years… more
- Lilly (Indianapolis, IN)
- …better for people around the world. The purpose of the Associate Director / Director Clinical Delivery Capabilities role within Exploratory Medicine and ... for successful delivery of the portfolio and clinical trials, the Associate Director / Director possesses the business acumen, process knowledge, and influence… more