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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.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Collaborate with Charles River Laboratories project leadership and Logica™ capability leads (chemistry, data sciences, DEL, in vitro pharmacology, ADME) to develop individual project strategic operating plans, including budget, resourcing, timeline, and milestone details, as well as both internal and client-facing documentation and presentations.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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PhD Immunology, Pharmacology, Oncology, or closely related discipline. PhD Immunology, Pharmacology, Oncology, or closely related discipline. Develop marketing and branding strategies for new and existing mouse models and preclinical services.
$100,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Strong knowledge of preclinical research, pharmacology, toxicology, and clinical development processes. Extensive experience (12+ years) in the biotech or pharmaceutical industry, with a focus on non-clinical and clinical development, required for immuno-oncology, preferred for infectious diseases.
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A working knowledge of biostatistics, translational sciences, clinical pharmacology, scientific and other technical disciplines and processes intimate with the drug development process. Provide scientific, clinical development and medical input into all other program documents in support of the development plan, including but not limited to study protocols, the investigators’ brochure, regulatory filings and submissions, abstracts, manuscripts and publications, clinical study reports, clinical pharmacology/translational medicine plans, etc.
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Two years clinical experience in a medical setting, demonstrate general medical and pharmacology knowledge – Required. A clinical degree (e.g., RPh/PharmD, BSN, RN) – Required. Prior experience in drug safety within the pharmaceutical or biotechnology industry.
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Understanding and application of pharmacology, chemistry and non-clinical toxicology to effectively inform the conduct of safety surveillanceAbility to thrive in a fast-paced environment while providing appropriate attention to detail.
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