- AbbVie (North Chicago, IL)
- …is to function as GLP Study Director for AbbVie internally conducted toxicology studies (80% of time) and external sponsor monitor for studies ... role designs, conducts and reports non-GLP and GLP general toxicology studies in support of drug submissions...with or without post-doctoral training and 0+ years of toxicology study director experience in… 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
- Charles River Laboratories (Reno, NV)
- …* Work closely within a small team environment. * Under direction of the study director , receive, review and accept proof corrections from report coordination ... protocols, amendments and report text. Provide comments and/or suggested changes to study director . * Upload data/reports to CR Sponsor portal and/or Sponsor… 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
- Charles River Laboratories (Spencerville, OH)
- …Responsible for overseeing study conduct of preclinical efficacy and/or toxicology studies assigned by TFM within safety assessment. Responsible for ... **Job Summary** We are seeking a **Research Scientist I, Study Director ** for our In Vivo team...state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored… more
- Charles River Laboratories (Mattawan, MI)
- …services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and ... these platforms/assays, the team is for execution of preclinical studies in small and large animal models in both...animal models in both regulated and non regulated preclinical studies . **Job Qualifications** + Bachelor's degree (BA/BS) with 7-9… more
- Amgen (Washington, DC)
- …toxicologists, providing expert analysis and interpretation of clinical pathology findings from toxicology studies . The candidate will be familiar with working ... the lives of patients while transforming your career. **Veterinary Clinical Pathology Director ** **What you will do** Let's do this. Let's change the world.… more
- Battelle Memorial Institute (Columbus, OH)
- …Toxicologist functions as a subject matter expert within the organization and, as a study director , has oversight of the scientific elements of projects to ... responsible for the organization, management, and business performance of non-clinical toxicology studies . Develops and implements strategic business and market… more
- Michigan State University (East Lansing, MI)
- Working/Functional Title Director Position Summary The College of Veterinary Medicine, Michigan State University, invites applications for the position of ... Director of the Veterinary Diagnostic Laboratory (VDL). The VDL is a premier, state-of-the-art veterinary diagnostic laboratory, accredited by the American… 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
- Otsuka America Pharmaceutical Inc. (Columbus, OH)
- …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
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …evaluation support and immunopathology oversight for GLP toxicology and PK studies of REGN molecules. The Associate Director will be expected to ... Regeneron is looking for an Associate Director of Pathology. **A typical day in this...drug development. + Perform pathology peer review of REGN toxicology studies at CROs (and therefore must… more
- State of Massachusetts (Lawrence, MA)
- …a highly experienced and dynamic environmental laboratory professional to serve as Director of the Division of Environmental Laboratory Sciences (DELS) and of the ... Laboratory, Environmental Organic Chemistry Laboratory, and Environmental Microbiology and Toxicology Laboratory - that generate scientific information/data from the… 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
- Bayer (Cambridge, MA)
- **Senior Director Clinical Pharmacology Lead** The Clinical Pharmacology Lead (CPL) Oncology will bring an extensive experience and knowledge of the Clinical ... TASKS AND RESPONSIBILITIES** The primary responsibilities for this role Senior Director Clinical Pharmacology Lead are to: + Independently represent Clinical… more
- AbbVie (Irvine, CA)
- …team members. + Understands and applies pharmacology, immunology, dermatology, anatomy and toxicology as needed to advise clinical study design and ... focus on safety planning and monitoring, from early development to post-market studies . + Contributes to the review of scientific content of protocols, Investigator… more
- Bristol Myers Squibb (Cambridge, MA)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . Associate Director and Group Leader, Oncology Discovery Biology The Oncology Thematic ... innovation, and business opportunities. **Position Summary** The role of Associate Director , Oncology Discovery Biology within the Oncology TRC at BMS involves… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …preparation/review of related key documents (ie protocols, Investigator's Brochures, clinical study reports, summaries for regulatory submissions). The Director , ... Director Clinical Development - Respiratory Date: Apr 29,...all phases of clinical research. The individual will oversee study teams and will be responsible for leading cross-functional… more
- Gilead Sciences, Inc. (Foster City, CA)
- …certain projects. These activities include, but are not limited to, clinical study design and protocol preparation, additional study or investigator ... documentation, contributions to data analysis plans, ongoing data interpretation, study reporting, and clinical development inputs into regulatory documentation,… more
- University of Utah (Salt Lake City, UT)
- Position Information **Position/Rank** Director of the Center for Medical Cannabis Research (CMCR) **Department** 00223 - Family and Preventive Medicine **City** ... **Details** **Center for Medical Cannabis Research ( CMCR ) Director ** The University of Utah is seeking a nationally...ability to leverage resources from the Center for Human Toxicology ( CHT ). **Location:** Located in metropolitan Salt… more