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The Histology Technician will work in our Anatomic Pathology department and will join a staff of highly trained scientists and technicians, and state of the art facilities to support our clients toxicology, safety pharmacology, and inhalation research programs.
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Our custom research and development approach is designed to integrate into services, including platform bridging, GLP toxicology material, and GMP manufacturing. The Quality Control Analytical Scientist II will develop, qualify, and perform analytical methods that are used to test and characterize GMP Raw Materials, In-Process Samples, Drug Substance and Drug Products.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Conduct GLP and non-GLP genetic toxicology assays (i.e. Ames, Comet, and micronucleus assays) Skills:Some combination of genetic toxicology and/or molecular biology laboratory skills.
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Provides strategic and operational direction ensuring that toxicology studies are conducted in line with the appropriate guidelines and regulatory test standards (FDA, WHO, GLP, and ISO.
$366,875 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Critically evaluate toxicology results and provides timely strategic advice to project teams and senior management on the potential impact of toxicology results on Program and Clinical/Regulatory strategy ·Oversee and provide direction in the preparation of Safety Pharmacology and Toxicology sections of regulatory documents (IND, CTA, NDA, briefing books, Investigator Brochures, etc.
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Ensures that toxicology studies and programs are conducted in accordance with the appropriate guidelines and regulatory test standards (FDA, WHO, GLP, and ISO). Senior Scientific Director, Toxicology About the Role:As a Sr. Leader, executes the strategic direction of the Toxicology function.
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Looking for an Executive Director, Toxicology with strong Leadership experience. Oversees and evaluates protocol preparation for toxicology studies. Oversees and directs the activities of the Toxicology group.
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We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
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Safety, efficacy, and toxicology unit (ASET) was launched as a preclinical CRO that spun out of Battelle in 2021 to address the changing needs of commercial organizations developing modern therapeutics.
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Oversees the adherence to all SOPs for Toxicology. Represent Preclinical Development on discovery and development-stage program teams ·Develops critical insights from data summaries and shapes presentations of results to peers, colleagues and Company Management.
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Lead and/or manage the design, monitoring, and interpretation of In Vitro, In Vivo, or pre-clinical bio-compatibility studies conducted under Good Laboratory Practices (GLP). Interpreting the results of Biological/Volatile Organic Compound tests for impacts to patient safety and preparation of expert reports on toxicology/patient risk in the support of regulatory documentation.
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Represent Preclinical development on discovery and development teams and regularly interfaces with internal and external colleagues to ensure timely and accurate dissemination of Safety Pharmacology and Toxicology findings.
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You have a minimum of a Bachelor’s degree in Toxicology or related fields (Required), MS or PhD desired. About Philips:We are a health technology company. JOB DESCRIPTION Job TitleSenior ToxicologistJob DescriptionExciting 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 Today - UpvoteDownvoteShare Job
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Understanding of general in vivo AAV pharmacology and toxicology best practices. The Study Manager will work cross-functionally with internal program teams and CROs. Responsibilities Primarily responsible for selecting, contracting, and monitoring non-GLP and GLP nonclinical studies with Contract Research Organizations (CROs), expert consultants and academic collaborators.
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This role will lead the safety strategy, from discovery through both nonclinical and clinical stages, and direct all phases of early investigative toxicology and in vivo non-GLP and GLP toxicology studies, in collaboration with project teams, CROs and consultants.
$220,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago
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