- Merck (Indianapolis, IN)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... regulatory requirements, and health literacy principles. **With minimal oversight, the Senior Informed Consent Medical Writer:** + Demonstrates… more
- Merck (Indianapolis, IN)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... regulatory requirements, and health literacy principles. With oversight, the Informed Consent Medical Writer: + Demonstrates growing independence managing… more
- Lilly (Indianapolis, IN)
- …requirements for study initiation and conduct (ie, ethical review board, informed consent , regulatory approval/notification) consistent with Good Clinical ... clinical experience, the Cardiometabolic Health Business Unit - Global Medical Affairs Sr . Director is an integral...trials (for example, phase I and II trials). The Senior Director is responsible for the planning, startup and… more
- Lilly (Indianapolis, IN)
- …determined to make life better for people around the world. **Responsibilities:** The Senior Medical Director is delegated various responsibilities by the ... while supporting the management team in fulfilling corporate goals and initiatives. The Senior Medical Director will provide strong leadership and ability to… more
- Lilly (Indianapolis, IN)
- …on and reviews scientific content of clinical documents such as protocols, informed consent documents, final study reports, and submissions (eg, annual ... project timeline. + Provide protocol oversight and input into informed consent documents. + Supports the monitoring...of others. + Support the management team, including the Sr . Director- Medical , in preparation and administration of… more
- Lilly (Indianapolis, IN)
- …on and reviews scientific content of clinical documents such as protocols, informed consent documents, final study reports, and submissions (eg, annual ... project timeline. + Provide protocol oversight and input into informed consent documents. + Supports the monitoring...of others. + Support the management team, including the Sr . Director- Medical , in preparation and administration of… more
- Sumitomo Pharma (Indianapolis, IN)
- … safety subject matter expert (SME) on behalf of PVRM for: Study Protocols, Informed Consent Forms (ICF), Safety Management Plans (SMP), Clinical Study Reports ... signal evaluation reports according to established safety governance policies and keeping senior leadership informed of safety issues. **Job Duties and… more