- 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 and capabilities supporting clinical development....strategies, integrations, and improvements for systems and capabilities. The Associate Director is responsible for collaborating with… more
- Lilly (Indianapolis, IN)
- …creative solutions to support communities through philanthropy and volunteerism. The Associate Director Clinical Development, Oncology independently leads ... quality, on time, and within scope and budget. The Associate Director consistently demonstrates leadership and influence...Understand the scope of work required to complete the clinical trial successfully. Monitor the status and… more
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. Purpose: 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
- IQVIA (Indianapolis, IN)
- **MSL Associate Director ** We are excited to announce that currently we are looking for **Medical Science Liaison Associate Director and Player-Coach** ... will provide peer-to-peer educational dialogue in support of the clinical trial teams. In addition, you will...inform decision making on various aligned teams. The **MSL Associate Director & Player Coach** will have… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …academic translational clinical research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for Director and 6-9 years ... While not essential, prior personnel management experience, will support position at entry ( Associate Director / Director ). + An advanced understanding of drug… 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)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director Process Engineering provides leadership and...site evolves from a design concept to a GMP clinical trial site. **Key Responsibilities:** + Responsible… more
- Lilly (Indianapolis, IN)
- …days remote - a generous relocation package can be included with offer The ** Associate Director - Submission Data Delivery** role leads all aspects of global ... data archiving, data standards, and submission process. **Responsibilities:** The Associate Director -Submission Data Delivery provides technical leadership and… 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 - Small Molecule Operations is directly responsible for managing the day-to-day manufacturing operations Small Molecule and… more
- Lilly (Lebanon, IN)
- …trials located in Lebanon, IN. This facility is Lilly's largest investment in a clinical trial manufacturing capacity and is intended to provide APIs for current ... molecule medicines at multiple scales as well as high potency antibody drug conjugates. Associate Director for Small Molecule Process Quality will lead the team… more
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