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Job Description AECOM has an opening for a Risk Assessor/Toxicologist in our Oakland or Sacramento California office to assist with a variety of projects including data management, site investigations and remediation.
$80,000 - $90,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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J.S. Held is a global consulting firm that combines technical, scientific, financial, and strategic expertise to advise clients seeking to realize value and mitigate risk.
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We are seeking a Pharmacologist/Toxicologist Lead with a strong scientific background to join our team, based remotely in Princeton, NJ. This role plays a crucial part in applying scientific methodologies to overcome challenges in pharmacology and toxicology, leading developmental programs, conducting risk assessments, and representing the company in meetings with global health authorities.
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Upon hire: California Clinical Toxicologist Scientist License Or. The Clinical Laboratory Scientist is responsible for specimen processing, test performance, test result reporting, and clerical and patient care support services.
$44.77 - $72.26 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Associate Director, Toxicology - Cell & Gene Therapy Are you a seasoned Toxicologist ready to influence the future of Cell & Gene Therapy (CGT)? Associate Director, Toxicology - Cell & Gene Therapy Are you a seasoned Toxicologist ready to influence the future of Cell & Gene Therapy (CGT.
$150,000 - $200,000Part-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As a Toxicologist, you will be responsible for designing, overseeing, and interpreting toxicology studies, leading a team of scientists, and serving as a key point of contact for clients. We are seeking a highly skilled and experienced Toxicologist to join our team of experts.
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Your New Chapter Awaits:As a Senior Study Director in the CGT department, you’ll play a pivotal role in advancing the science that keeps us all safe. Interface with different teams, including in vivo scientists, QC/QA, Account Managers/Sales, and the veterinary staff.
$150,000 - $200,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience with GLP (Good Laboratory Practice) and non-GLP toxicology studies. Knowledge and experience in cell and gene therapy programs are preferred. Your Credentials: Ph. D. in Toxicology, Pharmacology, or a related field.
$150,000 - $200,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Analyze and interpret study data, draw meaningful conclusions,make recommendations, and prepare comprehensive toxicology reports for clients and regulatory submissions. Key Responsibilities: Lead the design and planning of toxicology studies, including selecting appropriate study models and endpoints.
$150,000 - $200,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Your expertise will guide critical toxicology studies from conception to conclusion, ensuring excellence and integrity at every step. Act as the primary subject matter expert for clients, understanding their needs, providing advice, and addressing their toxicology-related inquiries and concerns.
$150,000 - $200,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As Toxicologist/Scientist, you are the scientific expert assessing and ensuring the safety of dsm-firmenich products according to the international legislations and regulations. Certification or in the process of acquiring certification as toxicologist (DABT and/or DABT.
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The Product Safety Toxicologist will report directly to the Regulatory Affairs Director. We are seeking an experienced regulatory toxicologist as a Product Safety Toxicologist for our global Regulatory Affairs organization.
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We are on the lookout for an exceptional individual to lead our client’s toxicology studies. A minimum of 8 years of experience in toxicology, with a strong track record in designing and overseeing toxicology studies.
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If you're passionate about safeguarding product safety and thrive in providing expert guidance, this is your opportunity! Board certification in toxicology (e.g., DABT). Previous experience in a CRO or pharmaceutical/biotechnology industry.
$150,000 - $200,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Work in close collaboration with the Genmab NonClinical Safety Lead/project toxicologist, other scientists, QA, and the CRO Study Director to generate GLP and non-GLP Study Plans for. The Nonclinical Safety & Toxicology Team are looking for an experienced toxicologist for a newly created position as sponsor monitor for nonclinical safety studies with Genmab’s pharmaceutical drug candidates outsourced to our CRO laboratory partners.
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