- Kymera Therapeutics (Watertown, MA)
- …and execute GLP, non-GLP, investigative, and in vitro studies With internal Study Monitor support, oversee toxicology studies for appropriate conduct, ... and plans for programs in all stages of drug development Oversee toxicology and safety pharmacology studies at multiple Contract Research Organizations… more
- 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
- RPM Research (San Diego, CA)
- … Study Directors, as well as others, and may serve as Study Director for in vivo CGT studies as needed, especially in client communication and questions. ... leadership and technical direction for in vivo effectiveness and toxicology CGT studies at preclinical programs. Guide...multidisciplinary group of 8 Ph.D. scientists. Provide guidance for Study Director in other focus areas Recommend… more
- RPM Research (Everett, WA)
- …3+ years of experience as a Study Director for in vivo studies (GLP experience required). Background in toxicology is a plus. Strong data analysis and ... Study Director - Research Scientist Your... Study Director - Research Scientist Your New Company! At...and impactful. Key Responsibilities Oversee the technical conduct of studies and represent the single point of study… more
- Legend Biotech US (Somerset, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking a Director , Preclinical Project Development and Strategic Lead as part of the Early-stage ... to advance Legend drug development efforts. Key Responsibilities Preclinical IND enabling study oversight Work closely with program teams to develop preclinical IND… more
- Cresilon, Inc. (Brooklyn, NY)
- …Preclinical Research Operations, including but not limited to in-vivo study design (Safety and Efficacy/Functionality evaluations), Preclinical Research Management, ... activities related to the design, initiation and follow-up of studies to support approval of Class I-III medical devices....of Class I-III medical devices. Develop, write, and/or review study protocols and reports. Act as technical mentor for… 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
