- Lilly (Indianapolis, IN)
- …life better for people around the world. **Position Description:** The Clinical Trial (CT) Supply Management Associate Director will provide operational ... to improve performance and speed drug development. **Responsibilities:** + Deliver improved clinical trial supply chain performance, assess and mitigate risk,… more
- Lilly (Indianapolis, IN)
- …and information to enable clinical development and speed medicines to patients. The Associate Director CTF Product Owner in Trial Management Systems will ... around the world. Purpose: Trial Management Systems as part of Clinical Trial Foundations (CTF), within Clinical Design, Delivery and Analytics (CDDA),… more
- Lilly (Indianapolis, IN)
- …policy and guidance to speed the delivery of medicines to patients globally. The Associate Director - Clinical Results Reporting Systems role requires broad ... to make life better for people around the world. Clinical Trial Foundations as part of ...Tech@Lilly, and other components of the R&D organization, the Associate Director - Results Reporting Systems is… more
- Lilly (Indianapolis, IN)
- …of ICH and quality guidelines needed for successful delivery of the portfolio and clinical trials, the Associate Director / Director Relationship Manager ... for people around the world. The purpose of the Associate Director / Director Relationship Manager role...of ICH and quality guidelines for successful portfolio and clinical trial delivery. + Strong business acumen,… more
- Takeda Pharmaceuticals (Indianapolis, IN)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Programming in Cambridge, MA, where you will oversee and ... & Quantitative Sciences team, you will report to the Director , Programming. Takeda SQS is looking to add individuals...**contribute:** + Oversee and direct the work of the Clinical trial disclosure programming team (within the… more
- Takeda Pharmaceuticals (Indianapolis, IN)
- …to the best of my knowledge. **Job Description** **About the role:** ** Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Oncology ... you will be a vital contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing and Systems (NRWS) Department… more
- Lilly (Indianapolis, IN)
- …4. Scientific data dissemination and exchange * Oversight of timely dissemination of clinical trial data. * Oversight of the critical analysis of data ... to support communities through philanthropy and volunteerism. **Purpose:** The Associate Vice President (AVP) - Cardiometabolic Health Global Medical Affairs… more