- Takeda Pharmaceuticals (Indianapolis, IN)
- …executes a labeling implementation plan to incorporate new scientific, safety and clinical data, as well as Health Authority responses / feedback into CCDS, USPI ... to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the development… more
- Prime Therapeutics (Indianapolis, IN)
- …and ability to adjust focus **Reporting Structure** + Reports to a manager or director in the Clinical Operations, Contact Center, Network Management or PBM ... SOP development and maintenance, and development and maintenance of audit protocols. **Responsibilities** + Participate in Regulatory Review Committee Meetings,… more
- Lilly (Indianapolis, IN)
- …the medicines needed for clinical trials (CT). As the PRD QA Sr. Director - CT Materials Supply and Centralized Services, you will lead the team responsible for ... oversight on quality-related matters and compliance across multiple areas ( Clinical Trial Materials, Wholesalers, Ancillary Supplies, and Chemistry Manufacturing and… more