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The Senior Scientist, Toxicologist will partner with the Vice President of Toxicology to develop and carry out the overall toxicology strategy for programs in both Discovery and Development. The Toxicologist will collaborate with external vendors, the internal preclinical pharmacology and toxicology team, and other stakeholders across the company to ensure efficient processes that scale with Verve's continued growth.
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The Senior Toxicologist will be responsible for building the overall toxicology strategy as well as targeted toxicology packages to support regulatory submissions for Centessa’s Orexin Agonist small molecule drug discovery programs from IND to NDA. The successful candidate will have substantial experience in CNS drug development with the knowledge and ability to contribute effectively to cross-functional drug development teams.
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Gradient, a Geosyntec Company, is seeking Early-Career Medical Device Toxicologist to assist colleagues and clients in toxicological risk assessments and biological safety evaluations for medical devices.
$110,000 a yearFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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We are seeking a Senior Scientist Toxicologist to join their preclinical pharmacology and toxicology team. We are seeking a Senior Scientist Toxicologist to join their preclinical pharmacology and toxicology team.
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QurAlis is seeking a highly motivated Toxicologist to support their toxicology strategy for successful development of the company’s lead molecules across all stages of development. Founded by an internationally recognized team of neurodegenerative biologists from Harvard Medical School and Harvard University, QurAlis is a clinical-stage biotechnology company advancing a pipeline with therapeutic candidates that target specific components of ALS and FTD pathology and defined patient populations based on both disease-causing genetic mutation(s) and clinical biomarkers.
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Ensure obtaining SOW, quotes, invoice management, POs and legal contracts necessary for consulting work with nonclinical safety experts/consultants as appropriate (safety pharmacologist, pathologist, genetic or reproductive toxicologist, biomarker expert etc.
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The incumbent (“Toxicologist”) will report directly to the Head of Nonclinical Safety, Translational & Bioanalytics and will be responsible for contributing to the design and conduct of nonclinical safety assessment programs, with emphasis on discovery/early and GLP toxicology study support, to enable progression of novel therapeutic agents through the drug development process, regulatory approval and post-marketing activities.
$175,000 a yearFull-timeExpandUpdated 3 days ago - UpvoteDownvoteShare Job
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The Principal Toxicologist will be responsible for the design and execution of nonclinical development toxicology studies conducted externally, interpretation and communication of the toxicology data/reports to support drug development decisions, and for summarizing and writing regulatory submissions.
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The Toxicologist will play a critical role in the assessment of the safety profile of small molecule drug candidates throughout the drug development process. The Toxicologist will play a critical role in the assessment of the safety profile of small molecule drug candidates throughout the drug development process.
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Collaborate with toxicologist and preclinical pharmacology scientists to design, analyze, interpret, and report preclinical PK and translational PK/PD studies to support candidate selection and IND filing, including human PK prediction to support starting dose and dose escalation schemes for first-in-human studies.
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10 years’ minimum experience as an occupational toxicologist in pharmaceutical/biotech/agrochem industry or consulting role. Director, Occupational Toxicologist. Experience in critical evaluation of occupational safety information from multiple sources, including in vivo, in vitro toxicological studies, pre-clinical and clinical studies.
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Identify gaps and risks; Oversee team of cross functional scientists supervised by Program Manager including bioinformatics scientists, and additional team members such as biologists, toxicologist in furtherance of drug discovery projects and; Oversee work of staff supervised by Program Manager applying bioinformatics tools and applications in areas including proteomics, transcriptomics, metabolomics, and clinical bioinformatics.
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Exciting opportunity to play an important role in improving and saving lives around the world through generating Toxicological Risk Assessments for Philips Sleep & Respiratory care devices/products, ensuring they are safe for use by the intended patient population.
$158,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Coordinates toxicological risk assessments with toxicologist. The Engineer II may be tasked by the supervisor to mentor one or more entry level Engineer I employees. Coordinates toxicological risk assessments with toxicologist.
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Support client's Oncology’s Head of NSE/toxicologist, as needed. Support client's Oncology’s Head of NSE/toxicologist, as needed. Primary responsibility for the Scientist/Senior Scientist in NSE is to ensure timely and high-quality deliverables from NSE to meet client's Discovery and Development goals; these deliverables include management/coordination of contracts, study-related documentation (protocols/reports), and regulatory submission documents, and program-related documents (e.g., candidate nomination.
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toxicologist job in Cambridge, MA
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