- Lilly (Indianapolis, IN)
- …to enable clinical development and speed medicines to patients. The Associate Director , CTF Product Owner in Trial Management Investigator-facing ... people around the world. Trial Management Systems as part of Clinical Trial Foundations (CTF), within Clinical Design, Delivery and Analytics (CDDA),… 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
- 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
- Lilly (Indianapolis, IN)
- …to support communities through philanthropy and volunteerism. **Purpose:** The purpose of the Associate Director - Data Standards role is to be responsible for ... providing technical leadership and ownership for data standards across the clinical trial dataflow. The main responsibilities of this role are: + Developing… 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)
- …make life better for people around the world. **Purpose:** The purpose of the Associate Director , DMC Expert role is to provide technical leadership and support ... effectively influence the direction of a program. + Communication skills in complex clinical trial environments + Some travel may be required (0 - 5%) Lilly is… more
- Lilly (Lebanon, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... clinical supplies and will therefore construct a new campus to manufacture Clinical Trial (CT) Active Pharmaceutical Ingredient (API) to meet needs for an… 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
- Bristol Myers Squibb (Indianapolis, IN)
- …team, RayzeBio aims to be the global leader in radiopharmaceuticals. **Summary** The Associate Director of Chemistry, Manufacturing & Controls (CMC) - Quality ... assigned. + Member of CMC Development Teams providing Quality (QA) input from pre- clinical to end of product life cycle including NDA filing, other market filings,… 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. **Position Description:** The Associate Director -Warehouse Operations will be engaged in the delivery of detailed design, creation of standard operating… more
- Grifols Shared Services North America, Inc (Indianapolis, IN)
- …safety data (toxicology) and use this information to develop safety mitigation strategies in clinical trial design + Serve as a key part of the cross-functional ... than 110 countries and regions. **Position Overview:** The Medical Director will be responsible for clinical strategy... research experience with at least 5 years of clinical document production and/or clinical trial… more
- Lilly (Indianapolis, IN)
- …finalization of CMC documents for global regulatory submissions, including Clinical Trial Applications, Market Authorization Applications, post-approval ... to make life better for people around the world. **Purpose:** The Senior Director of Global Regulatory Affairs - CMC (GRA-CMC) leads and manages the scientific… more