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The ideal candidate will play a critical role in leading and managing toxicology studies as a senior study director within CGT department, ensuring the safety of products and substances, and providing expert toxicological guidance to clients.
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Board certification in toxicology preferred (, DABT, ERT) Experience in a GLP preclinical environment preferred. This position will function within the Toxicology Unit of Corporate Preclinical Development and Toxicology (CPDT) and will support the conduct of nonclinical laboratory investigations of medical devices and materials in accordance with GLP regulations and the Client CPDT Quality System.
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You will work with experienced pharmacometricians, Preclinical Pharmacokinetics, Drug Metabolism, Toxicology, and Clinical Pharmacology colleagues to provide inputs to overall product development plans and to address research and development objectives and issues.
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Extensive knowledge of cell therapy concepts and exploration, including in vitro and in vivo study experience. Prepare necessary documentation for project reviews (proposals, monthly, quarterly, annual, or study reports), patent applications, publications, and/or animal, biosafety, or human subject protocols.
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The Scientist I, In Vitro Pharmacology will play a key role in the pre-clinical pharmacology and toxicology team conducting in vitro studies to support in vivo tLNP-CAR product candidate testing, optimization and development for various indications including autoimmunity, fibrosis or oncology.
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Summer Intern position in the Cellular & Molecular Toxicology Group will be focused on in vitro cellular respiration studies. Present study design & interpreted data at the end of the internship period.
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Bachelor’s degree in Physical Education, Exercise Science, Education with an emphasis in Physical Education, Kinesiology, Physiology of Exercise, or Adaptive Physical Education AND Master’s degree in any life science, Dance, Physiology, Health Education, Recreation Administration, or Physical Therapy ANDfifteen (15) semester units of upper division or graduate study in adapted physical education; OR,3.
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The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
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Give Campus Ministers an understanding of the importance of their work through study of retreat spirituality; Role Title: Retreat Coordinator & Theology Teacher Hours: Full-time. While Mater Dei has an already established curriculum, retreat program, and other faith-based ministries, the administration is open to re- imagining, through a strategic approach, a ministry design that effectively and deeply touches the lives of its campus community members with God’s presence.
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Educational background in bioengineering, chemical engineering, materials engineering, or similar field of study preferred. Lead projects in the microfluidics and surface chemistry areas to support the transfer and commercialization of products/processes, including development and implementation of surface deposition, metrology, and assembly processes.
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DESCRIPTIONThe UC San Diego Department of Visual Arts is one of the country's leading centers for study and research in art and art history. Reporting directly to the Department of Visual Arts Facilities Manager, the Gallery Technician and Preparator will manage all aspects of exhibition preparation across departmental spaces located in the Mandeville Center, the Structural Materials and Engineering building (SME), and the Visual Arts Facility.
$58,547 - $61,261 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Over the last twelve years, we have served major roles in high-profile projects in the water sector in San Diego including Pure Water Oceanside (Program Manager), VID Flume Replacement Alignment Study (Core Team Member), RMWD Groundwater Recovery Feasibility Study (Prime Consultant), City of Oceanside’s Advanced Metering Infrastructure Program (Program Manager), and more.
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Provide operational and strategic input into study planning and study specific documents such as synopsis, protocol, ICF, CRFs, CRF Completion Guidelines, Study Execution Plans, Clinical Data Review Plan, Clinical Database edit specifications, Clinical Study Report (CSR) development, etc.
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The candidate will be part of the Drosophila research team in the Panda lab carrying out experiments outlined in two federally funded grants to study the impact of nutrition and circadian rhythm on brain function using Drosophila models of human neurodegenerative diseases.
$70,000 - $77,500 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Candidates should hold an advanced degree in toxicology, environmental or chemical engineering, environmental health, environmental science, biology, chemistry, or similar field. Our staff is comprised of registered professionals in civil engineering, geology, hydrogeology, and geotechnical engineering.
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toxicology study jobs in La Jolla, CA
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