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Additionally, you will provide subject matter expertise in some of the areas of toxicology that include fit-for-purpose safety biomarker development and validation, bio-fluid/tissue biomarker analysis, in silico, genetic, endocrine, and reproductive toxicology efforts to support on-going development of preclinical candidates.
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Expertise in toxicology/pharmacology and determining health-based exposure limits. A doctoral degree in Toxicology, Pharmacology, or a related field; or a master's/bachelor's degree with significant experience in toxicology/pharmacology.
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Develop and maintain collaborative relationship with colleagues within the department, internal stake holders (i.e., DMPK, toxicology, biology, translational medicine, medical, clinical, biometrics, regulatory, clinical operations, CMC, etc.
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Serve as primary case manager for patients in SOF admissions process in collaboration with Admissions Coordinator, including, but not limited to, the following responsibilities: conduct pre-screening to assess treatment and evaluation needs for all patients referred; coordinate signing of Release of Information forms, acquire relevant medical records, and arrange for completion of toxicology screening; serve as point of contact for ongoing questions from the patient as they arise.
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Our client offers preclinical services for drug discovery, focused on the use of nonhuman primates to determine pharmacokinetics, pharmacology and toxicology of small molecules and biologics. 5+ years of experience in scientific sales in the Life-science industry (Toxicology, Pharmacology, Primates desired.
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Our complete workflow solutions enable productivity and efficiency for customers performing food and beverage testing and manufacturing, environmental and industrial testing, biopharma QA/QC, toxicology, and anti-doping.
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Senior Principal Scientist, Investigative Toxicology. A PhD in toxicology, pharmacology, biology, or equivalent scientific discipline is required, with a minimum of 8-10 years of relevant research experience in a pharmaceutical or biopharmaceutical setting.
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Working knowledge of all functional areas of exploratory development, including chemistry/biochemistry, biology, toxicology, CMC, translational medicine, early clinical development, regulatory, etc., and demonstrated ability to successfully and effectively cooperate, collaborate and work across functions.
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Strong understanding of all aspects of compound optimization including synthetic chemistry, structure-based drug design, ligand-based drug design, pharmacokinetics, pharmacology, and toxicology.
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PhD or MSc (with equivalent experience) in a relevant field (e.g., Biology, Biochemistry, Pharmacology, Toxicology, Engineering, Physics) Hands-on experience establishing and optimizing in vivo pharmacology models and assays.
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The product line responsibility includes Toxicology (Drugs of Abuse products), Capital Equipment, MAS Clinical Chemistry Controls, AcroMetrix Molecular Controls, ISD/TDM's product lines, and BioMarkers.
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Provide ongoing management, education, and support of patients in all phases of treatment including nursing visits; medication management; storage, monitoring, and administering controlled medications; administration and interpretation of urine toxicology screens, integration with primary care and behavioral health, linkage and coordination with external programs, medication teaching, supportive counseling, and medication refills.
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Responsible for all areas of preclinical research and development, including generating pharmacology and toxicology data, preclinical trial strategy and design, preparation of the preclinical development plan to support successful INDs, and contribution to regulatory strategy.
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III. A Graduate degree with a major in environmental science, biology, chemistry, earth science, environmental health, meteorology, natural science, toxicology or public health may be substituted for a maximum of three years of the required (A) experience and one year of the required (B) experience.
$80,471.56 - $118,539.98 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Takeda Development Center Americas, Inc. is seeking a Senior Manager, Clinical Data Management in Lexington, MA with the following requirements: Master’s degree in Pharmaceutical Sciences, Pharmacology or Toxicology or related field or foreign academic equivalent plus 6 years of related experience.
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toxicology job in Cambridge, MA
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