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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 7 days ago - UpvoteDownvoteShare Job
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The Anatomic Pathology Technician will join a staff of highly trained scientist and technicians, and state of the art facilities to support our clients’ toxicology, safety pharmacology, and inhalation research programs.
ExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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In-depth experience with designing, conducting, and evaluating non-GLP and GLP non-clinical studies within toxicology and/or safety pharmacology, preferably with experience with siRNA/oligonucleotides.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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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.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Oversee and provide strategic direction for Toxicology/Pathology, BioAnalytical/DMPK, Biomarkers, and Clinical Pharmacology teams to ensure robust support for clinical development programs. 12+ years of experience in the biopharma industry in non-clinical development (toxicology, pharmacology, pharmacokinetics, bioanalytical sciences, or related discipline.
$300,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Knowledge of laws, regulations, policies and guidelines that govern animal research, research conduct principles (GLP) and current methodology of laboratory animal medicine and management is important.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Brings decades of experience to accommodate a wide variety of GLP and non-GLP studies in all in vivo models and dose routes. Carcinogen Use, Laboratory Animal Handling, National Toxicology Program (NTP) work, Personnel Air Purifying Respirator usage (including "dust mast" and PAPR), Blood borne Pathogen and/or Infectious Waste Handling.
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Understand the impact of DMPK/BA and interdependencies with other functional teams within the enterprise including Pharmacology, Toxicology, Clinical and Regulatory disciplines. Experience reviewing regulatory documents, DMPK and BA reports, and non-GLP/GLP data and notebooks.
$59 an hourFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Partner with Drug Metabolism and Pharmacokinetic (DMPK) and Bioanalytical (BA) Subject Matter Experts (SMEs) to author, review and track regulatory documents. Job Description: POSITION Nonclinical Regulatory Document and Scientific Writer.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Job Title: Nonclinical Regulatory Document and Scientific Writer. At minimum, a Bachelor’s degree in Chemistry, Biology or related science with a strong background in DMPK and BA including knowledge of the FDA GLPs.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Partner with Preclinical Development Drug Metabolism and Pharmacokinetics (DMPK) and Toxicology departments to ensure GLP compliance. You will be responsible for QA oversight and support of both in-house GLP bioanalytical laboratories and outsourced bioanalytical and toxicology studies, ensuring compliance with relevant regulatory requirements and company SOPs.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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About ASET West Jefferson, OH : AmplifyBio’s 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.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Experience in executing non-GLP and GLP pharmacology and toxicology studies to support regulatory filings. Manage the In Vivo Pharmacology Team, vivarium operations and pre-clinical in vivo studies execution.
$180,000 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Actively leads/ participates on project teams by advising on GLP, GLP OECD, and related matters as the preclinical quality team lead on global programs, executes quality assurance activities for GLP toxicology studies and pre- clinical/ clinical bioanalytical assay method validation and sample analysis including review of study protocols/ plans, reports, and data, documents for regulatory submissions, providing solutions when challenges arise.
$195,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The areas of focus include Medicinal Chemistry & CDMO, Drug screening, DMPK, Safety Toxicology and Bioanalytical services. Solid knowledge of CRO, Biotech and Pharma industries with a grasp on bioanalytical, both GLP and non-GLP studies.
Full-timeExpandApply NowActive JobUpdated 16 days ago
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