- Tris Pharma (Monmouth Junction, NJ)
- …inform key development decisions.Designs non-clinical in vitro and in vivo pharmacology/ toxicology /translational studies . Analyses and reviews data to inform ... success.We have an opening in our Monmouth Junction, NJ Facility for a Director , Clinical Pharmacology. The Director , Clinical Pharmacology is responsible for… more
- Insmed Incorporated (NJ)
- …and for the future of science, we're in. Are you?About the Role:The Sr. Director CMC QA will lead QA CMC oversight for drug products, biologics, and combination ... product programs from toxicology through Phase 3. This role ensures phase-appropriate GMP...trial materials, including DS/DP used in early and late-phase studies .Oversee QA support for development-stage manufacturing, analytical, and, including… more
- Editas Medicine (Cambridge, MA)
- …pipeline. + Lead the design and oversee execution of GLP and non-GLP toxicology studies to support regulatory submissions and interactions with health ... therapies to patients with genetic disorders. Characterizing Your Impact: As the Director , Toxicology you will: + Develop phase-appropriate nonclinical safety… more
- Lilly (Indianapolis, IN)
- …closely with cross-functional teams to ensure the successful execution and interpretation of toxicology studies . **What we are looking for:** + A skilled and ... for compounds moving into development. + Plan, organize and oversee Discovery Toxicology studies from initiation to completion, ensuring adherence to deliverable… more
- Fresenius Medical Center (Ogden, UT)
- **Your Purpose:** As Director of the Global Biocompatibility and Toxicology Competence Center, you will be responsible for establishing and leading a globally ... tasks:** + Build, lead, and develop the Global Biocompatibility and Toxicology Competence Center, both professionally and disciplinarily. + Derive overarching… more
- Bill and Melinda Gates Foundation (Seattle, WA)
- …development and to the market. + Proven expertise in GLP-compliant toxicology study design, interpretation, and regulatory documentation (eg, IND/CTA/NDA/BLA ... We are currently seeking a Senior Program Officer (SPO), Toxicology , to join the Translation Sciences (TS) team within...decrease the likelihood of later safety failures in human studies . The ideal candidate brings deep expertise in the… more
- Charles River Laboratories (Ashland, OH)
- …regulatory compliance of these projects. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Serve as a study director in the direction and execution of assigned studies ... nonclinical research studies of basic to moderate complexity, to include study management, interpretation and reporting of study data, and assuring the… more
- University of Miami (Miami, FL)
- …has an exciting opportunity for a Supervisor, Laboratory Services in the Toxicology Lab. SUMMARY The Supervisor, Laboratory Services provides technical direction and ... of medical students and allied technical personnel through specialized studies , scientific committees, and collaborative research. + Establishes and continuously… more
- Penn Medicine (Philadelphia, PA)
- …of Pathology and Laboratory Medicine is seeking a Medial Laboratory Scientist in Toxicology at the Hospital of the University of Pennsylvania (HUP) to join their ... actions taken including calling technical support. Immediately notifies Supervisor and/or Director if unable to resolve test system issue. Ensures test results… more
- Lilly (Indianapolis, IN)
- …have experience working in a GLP environment designing and supervising the conduct of toxicology studies ? The Nonclinical Study Management Team (NSMT) is a ... conducted externally at third party organizations (TPOs). To enable toxicology studies , study managers must... conduct at the TPO via communication with the Study Director and/or onsite observation, and real… more
