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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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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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Design and develop data capturing tools: Electronic Data Capture (EDC) Systems (Eg: iMedidata Rave and IBM Clinical) eCOA, IRT; Manage electronic Trial Master File (eTMF) QC review eg: Veeva Vault; Lead the Audit and Inspection/Submission Readiness activities like documentation of QC and preparing Storyboards (Eg: FDA/EMA Submissions.
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If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com.
$18 an hourExpandUpdated 4 days ago - UpvoteDownvoteShare Job
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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.
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Job DescriptionTakeda 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.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Expertise in either Biologics-related toxicology or developmental and reproductive (DART)-related toxicology. PhD or DVM with 10+ years of toxicology experience in the pharmaceutical industry or Master's in Toxicology with 15+ years of experience.
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Although each current member has a specific area of interest and responsibility, including: chemistry, toxicology and immunology; hematology and coagulation; point-of-care testing; flow cytometry; blood banking and apheresis; molecular testing; and microbiology, virology, and parasitology, there is significant overlap across sections, and all periodically cover the entire laboratory.
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III. A Graduate degree with a major in the field of 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.
$74,159.02 - $108,560.4 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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The candidate should possess an in-depth understanding of safety pharmacology, investigative and regulatory toxicology, and have experience designing and critically evaluating results of exploratory and GLP-compliant toxicology studies.
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You'll lead and oversee toxicology programs, from target identification to GLP (Good Laboratory. Organize and manage toxicology programs strategically, ensuring alignment with clinical development.
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Facilitate urine and toxicology tests by following protocol. Working knowledge of addiction treatment or related field preferred, but not required. Facilitate urine and toxicology tests by following protocol.
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Strong working knowledge of biochemistry, biophysics, ADME, pharmacokinetics, biology, pharmacology, DMPK, and toxicology. Head of Medicinal Chemistry and Head of the Novo Nordisk (NN) Small Molecule Research Unit. Will interact and closely collaborate with other Small Molecule Unit Scientists (chemists, biochemists, biophysicists, crystallographers), Data Science & Innovation (DSI) computational chemists, Global Drug Discovery (GDD) biology, Global Research Technologies (GRT), GDD Drug Metabolism and Pharmacokinetics (DMPK), cellular biology, pharmacology and translational medicine teams globally.
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Potential to read both non-GLP and GLP studies for toxicology studies (preferred) At least one year of fellowship training in an anatomic pathology subspecialty, or currently working to complete a year of fellowship training in a subspecialty.
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Based employees are also eligible to receive, per calendar year, up to. Company headquarters in Lexington, MA. Individual may reside anywhere in the U.S. Up to 100% remote work allowed from any location in the U.S.
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toxicology job Company: Charles River Laboratories in Wilmington, MA
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