- Takeda Pharmaceuticals (Cambridge, MA)
- …that will inspire you and empower you to shine? Join us as a Director , Quantitative Clinical Pharmacology Lead in our Cambridge, MA office. Takeda is a global, ... and experience with design, analysis, and reporting of clinical pharmacology studies . + Extensive experience in late-state drug development, regulatory submissions… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Comfortable working with and educating colleagues in drug metabolism, toxicology and clinical pharmacology departments, on strategies to understand drug ... design and execution of nonclinical and clinical radio- and non-radiolabeled ADME studies . Serve as an expert resource; to ensure radiochemical design, develop… more
- Charles River Laboratories (Reno, NV)
- …with sponsor on-site visits. Serve as primary point of contact to the sponsor when study director is not available. * Write initial protocol drafts. Upon ... study director approval, distribute draft protocols for...state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored… more
- WuXi AppTec (Cranbury, NJ)
- …Assumes complete responsibility for assigned projects, such as acting as study director / principal investigator, and assumes an executing responsibility ... for each assigned PKPD studies . Maintains the labs and program to AAALAC and...with accepted standards and practices. **Responsibilities** + Serve as Study Director , Principal Investigator, or Project Coordinator… more
- Lilly (Indianapolis, IN)
- …and payer); the product lifecycle plan, clinical strategies, development plans and study protocol design. + Contribute to business unit and global alignment of ... content of clinical documents such as protocols, informed consent documents, final study reports, and submissions (eg, annual reports) according to the agreed upon… more
- Charles River Laboratories (Mattawan, MI)
- …* May serve as a consultant in pathology-related issues. * May serve as a study director or principal investigator. * May function as a peer review pathologist ... services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and… more
- Charles River Laboratories (Mattawan, MI)
- …minimal oversight. + Function as a Principal Investigator, Individual Scientist and/or Study Director as assigned with minimal oversight. + Actively communicate ... services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and… more
- Charles River Laboratories (Stilwell, KS)
- …Works with cross-site team members to implement refinements. + In consultation with the Study Director is a contact for Sponsor discussion on veterinary care and ... services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and… more
- State of Colorado (Denver, CO)
- …accordance with HB 21-1266 and HB 24-1338, following the guidance of OEJ Director , the department's senior leadership, and the Governor's Office. The EECIA manager ... experience in Environmental justice research or programs, epidemiology or toxicology , environmental project management, and/or environmental community outreach and… more
- Abbott (Abbott Park, IL)
- …APAC regions to initiate and execute Health Economic analyses, Outcomes Research/RWE studies and Market Access initiatives to maximize and protect patient access ... to ensure the development of state-of-the-art Health Economic and Outcomes Research studies . Key internal customers may include global affiliate MA leads, new… more