- Eisai, Inc (Exton, PA)
- …the operation of the biologics pilot plant (whose purpose is to produce material for toxicology and phase I to III studies ), and in the late-stage processes at ... profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is responsible...for pre-clinical and phase I to phase III clinical studies , including the development of long-range planning and weekly… more
- Vera Therapeutics (Brisbane, CA)
- …programs. Work with CROs to supervise in vitro and in vivo pharmacology studies supporting Vera's INDs. Lead pharmacology and toxicology analyses for IND ... Job Description Title: Executive Director , Translational Research Biology Location: Brisbane, CA About...enabling studies . Collaborate with Research, Toxicology , CMC, Clinical Pharmacology, Bioanalysis, Project Management, CMC, and… more
- Eli Lilly and Company (Indianapolis, IN)
- …produce API for clinical trials (and possibly for non-GMP purposes such as toxicology studies ). This will include batch record creation/close out, process ... required throughout 2025 and 2026. Organization and Position Overview: The Senior Director Process Translation and Execution is directly responsible for managing the… more
- Eli Lilly and Company (Indianapolis, IN)
- …in vitro, in vivo, and in silico approaches to mechanistically study the pharmacokinetics, absorption, and disposition of biologics/antibodies. You will serve ... of scientifically integrated data packages to guide compound selection, study design, portfolio decisions, and regulatory submissions. *Partner with cross-functional… more
- Eurofins (St. Charles, MO)
- …Performs data and report QC review within the department, and may support study director . Takes ownership of client projects with minimal supervision. Supports ... advanced material sciences and in the support of clinical studies , as well as having an emerging global presence...a lab role. Conducts production assays primarily in ADME Toxicology Services, but will also support BioTherapeutics Services based… 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
- Battelle Memorial Institute (West Jefferson, OH)
- …work.** **Responsibilities** + Serves as Study Director on toxicology , biodistribution, pharmacokinetic, efficacy, and related studies for commercial and ... maintaining quality and compliance. The Toxicologist functions as a study director within the organization and has...scientific elements of projects to ensure successful implementation and/or study completion of toxicology studies .… more
- Pfizer (Andover, MA)
- …and characterization pertaining to OELs and ADE values + Experience of toxicology study design and internationally accepted testing guidelines (eg, Organization ... patients' lives. Working under the direction of the Sr. Director , Product Stewardship and with peers in the product...[OECD] Test Guidelines), and in the monitoring of contracted toxicology studies at external contract research organizations… 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
- Battelle Memorial Institute (Columbus, OH)
- …technology to solve complex global challenges. **Responsibilities** + Serves as Study Director for Inhalation Toxicology studies with focus on public ... Team, you will play a crucial role as a study director within the organization and has...scientific elements of projects to ensure successful implementation and/or study completion of inhalation toxicology studies… more
- Charles River Laboratories (Horsham, PA)
- …studies on basic levels of studies under the supervision of a study director , principal investigator and/or supervisor of study coordination. Assist ... 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 (Reno, NV)
- …shipping database. *Review study protocols and provide recommendations to study director /supervisor on technical and logistical aspects of protocol design. ... in conjunction with other departments to coordinate assignments to facilitate scheduling of study -related processes on assigned studies to ensure protocol or … more
- Lilly (Boston, MA)
- …for our partners and patients. **Purpose of the Role:** The Director [commensurate with experience], ExploR&D Translational Medicine incumbent is responsible for ... to develop, consult on, and/or execute development plans. + Workswith toxicology and pharmacokinetics teams, especially for First-in-Human (FIH) assets, in establish… more
- Charles River Laboratories (Reno, NV)
- …services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and ... a career that you can feel passionate about. **Job Summary** The Associate Director of Laboratory and Logistics position at Charles River Laboratories in Reno, NV… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …stratification and dose selection. + Provide medical oversight of early phase studies and oversee protocol development and study execution in collaboration ... products for the maintenance of everyday health. As a Director of Translational Medicine (TM), you will be a...any internal or external scientific communication related to clinical studies or mechanism of action of the study… more
- Otsuka America Pharmaceutical Inc. (Charleston, WV)
- …first-in-human, proof of concept (PoC), mass balance and drug interaction studies . The Director will author/review **clinical pharmacology** submission documents ... nutraceutical products for the maintenance of everyday health As a Director , Quantitative Pharmacology, **Clinical Pharmacology,** you will oversee all **clinical… more
- University of Utah (Salt Lake City, UT)
- Position Information **Position/Rank** Center for Medical Cannabis Research Director **Department** 00952 - Division of Epidemiology **City** Salt Lake City, UT ... a nationally recognized cannabis researcher, to serve as the Director of the Center for Medical Cannabis Research (...ability to leverage resources from the Center for Human Toxicology ( CHT ). **Minimum qualifications** : PhD, MD,… more
- Charles River Laboratories (Shrewsbury, MA)
- …services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and ... and advancement of scientific programs. o Contribute to problem resolution of study related science-based issues. o Provide scientists with guidance in the… more
- Amgen (Thousand Oaks, CA)
- …and transform the lives of patients while transforming your career. **Executive Director , Clinical Development, Rare Disease** **Live** **What you will do** Let's do ... the world. In this vital role as an Executive Director , you will play an important role in scientific...design and execution of Phase 2 through Phase 4 studies . They will serve as the principal representative for… more
- Sanofi Group (Morristown, NJ)
- …industry experience + **Minimum preferred skills:** experience as a GLP Study Director ; Certification by the American Board of Toxicology is preferred but ... entail formulating the nonclinical safety strategies, designing safety pharmacology and toxicology studies , authoring regulatory documents, being a member of… more
