- 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
- Bristol Myers Squibb (Devens, MA)
- …of a company-wide approach to perform GLP environmental fate/effects studies and environmental risk assessments according to appropriate international regulatory ... on diverse multi-functional teams to deliver on-time and on-budget GLP studies and environmental risk assessments necessary to support successful clinical trials… more
- Gilead Sciences, Inc. (Foster City, CA)
- …DMPK Biologics, providing PK or PK/PD expertise to the design of nonclinical PK, toxicology , or pharmacology studies . + Lead the DMPK strategy for programs at ... in support of project deliverables and first-in-human dose predictions. + Prepare study protocols and coordinate execution of nonclinical studies which may… more
- Grifols Shared Services North America, Inc (Fort Worth, TX)
- …in more than 110 countries and regions. **Position Overview:** The Medical Director will be responsible for clinical strategy relating to upcoming clinical trials, ... are not limited to the following:** + Design of trials, including study population and eligibility criteria, treatment duration, clinical endpoints, biomarkers, and… 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
- BeOne Medicines (Cambridge, MA)
- BeOne Medicines USA, Inc. (f/ka BeiGene) seeks Director , Regulatory Affairs in Cambridge, MA, USA: **Job Duties:** + Provides high level regulatory strategic and ... limited to general regulatory strategies, regulatory requirements for clinical studies and marketing approval in domestic markets, regulatory strategic development… more
- Astellas Pharma (Northbrook, IL)
- …external stakeholders as a member of the asset team and leader of the clinical study team to advance one or more clinical trials. Serves as Medical Monitor w/ ... responsibility for safety monitoring. + Ensures patient safety on clinical study is maintained. Generates safety related documents, such as medical monitoring… more