- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. Purpose: The Associate Director , Clinical Trial Foundations (CTF), will serve as ... the subject matter expert for clinical systems supporting clinical development. In this...and assisting the team to prepare for inspections. The Associate Director is responsible for collaborating with… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. **Purpose:** The purpose of the Associate Director Analysis role is to support the design of clinical ... disease prevalence, etc.), analyses and insights to drive excellence in clinical trial design, enabling more efficient planning and execution to speed medicines… more
- Sumitomo Pharma (Indianapolis, IN)
- …marketed products. + Conduct safety surveillance over product life cycle, reviewing clinical trial and post-marketing Individual Case Safety Reports (ICSRs), ... highly motivated, and experienced individual for the position of ** Associate Medical Director .** The Associate ...safety of clinical trials, including monitoring of clinical trial safety and laboratory data. +… more
- Lilly (Indianapolis, IN)
- …well as oversight of DS manufacturing at qualified collaboration partners. The Associate Director for Technical Services manages functional responsibilities for ... technical services, environmental monitoring and process microbiology groups within the Clinical Trial Bioprocess Pilot Plant, which is focused on producing bulk… more
- Lilly (Indianapolis, IN)
- …to enable clinical development and speed medicines to patients. The Associate Director - Results Reporting Systems role requires broad expertise of ... Tech@Lilly, and other components of the R&D organization, the Associate Director - Results Reporting Systems is...Sciences, CDISC Standards, and/or Data Management with respect to clinical trial data collection, analysis and reporting… more
- Lilly (Indianapolis, IN)
- …for people who are determined to make life better for people around the world. The Associate Director , CTF Clinical Results Systems (as part of Clinical ... processes and technology + Knowledge of emerging IT capabilities used for clinical trial data management + Capacity and workload management expertise + Strong… more
- Lilly (Lebanon, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director Small Molecule Process Engineering provides...site evolves from a design concept to a GMP clinical trial site. **Key Responsibilities:** + Responsible… more
- Lilly (Indianapolis, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director , Plant Engineering provides leadership and...management of critical and non-critical activities associated with GMP clinical manufacturing and all necessary support functions. + Ensure… more
- Lilly (Lebanon, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director -Automation Engineering is responsible for the supervision of the process control engineers and consultants that support the daily… more
- Lilly (Lebanon, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director -Automation Engineering - Control System Hardware, I&C, Projects and Site Support is responsible for the supervision of the… more