- University Of Vermont (Burlington, VT)
- …Medical Center is seeking a physician-scientist/academic clinician to serve as Associate Director of Clinical & Translational Research. The position is available at ... effort protected for scholarly activities. The latter may be laboratory-based investigations or clinically focused research. This position involves oversight and… more
- Catalent Pharma Solutions (San Diego, CA)
- Director of Quality Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and ... degree of operational excellence and a mature Quality Culture. The Site Quality Director will implement strategies and tactical objectives to move the site towards… more
- ASM Global (New York, NY)
- Job Title: Director , Litigation CounselLocation: NYC or Frisco, TXDepartment: LegalReports To: Chief Legal Officer LEGENDS GLOBAL Legends Global is the premier ... and brokers on coverage and claims handling.* Support internal investigations and pre-litigation dispute resolution.* Develop litigation protocols and reporting… more
- Lilly (Indianapolis, IN)
- …solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental impact. The Associate ... Director - Analytical Quality Assurance ensures that laboratory activities...or the integrity of data. + Coach/mentor others regarding investigations are conducted for deviations, stability failures and out… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Senior Director , Compliance & Ethics, Global R&D Date: Nov 22, 2025 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: ... regulatory environment surrounding non-promotional scientific exchange, pre-clinical and clinical trial conduct, pharmacovigilance requirements, health economic outcomes research, and… more
- Bristol Myers Squibb (Indianapolis, IN)
- …RayzeBio aims to be the global leader in radiopharmaceuticals . The Associate Director of Validation is responsible for leading the validation function to ensure ... and regulatory compliance. + Lead and mentor the deviation investigations team for the site. + Uphold all safety...in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency,… more
- Bristol Myers Squibb (Princeton, NJ)
- …issues and questions + Manage ad-hoc requests to ensure all questions and investigations are researched and responded to appropriately to the relevant stakeholders + ... + 5+ Years of relevant pharmaceutical experience for Associate Director + Experience interacting with marketing management, understanding, anticipating, and… more
- Bristol Myers Squibb (Devens, MA)
- …their personal lives. Read more: careers.bms.com/working-with-us . The **Associate Director , Product Technical Steward, Cell Therapy Technical Operations (CTTO)** is ... level, balancing agility and discipline. + Prior experience in leading cGMP investigations utilizing formal Root Cause Analysis tools strongly preferred. + Ability… more
- J&J Family of Companies (Spring House, PA)
- …regulatory nonclinical documents and health authority responses to support clinical trials and compound registrations. + Participate in medical safety teams, signal ... due diligence activities is preferred. + Previous experience as a Study Director /Study Monitor under Good Laboratory Practice (GLP) regulations is preferred. +… more
- AbbVie (North Chicago, IL)
- …appropriate and sound, consistent with the objective(s) of the scientific investigations + Demonstrate an excellent understanding of statistical concepts and ... related issues arising in the design, conduct or analysis of clinical trials or other scientific research. Independently select, evaluate and implement alternative… more