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Learn about the benefits of the assigned healthcare and pharmacology products in relation to the applicable therapeutic area or disease state. Technical & Pharmacology Knowledge. As a Pharmaceutical Sales Rep field professional, you have consistently met or exceeded sales and other critical business goals and metrics in a highly complex and competitive market.
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Good understanding of Anatomy and Physiology as well as Pharmacology. Experience: Completion of the MH Coder I apprenticeship program or 1-2 years' experience coding in an outpatient setting using 3M Coding and/or Optum Reimbursement encoder and CAC products.
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Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
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Pharmacology efforts that aim to elucidate novel drug target mechanisms and establish causal relationships between drug target modulation and disease. This position requires a Bachelor's degree in Cell Biology, Molecular Biology, Biochemistry, Physiology, or related field.
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PhD or MD/PhD in Molecular or Cellular Biology, Genetics, Pharmacology (or a comparable biological science) with 5+ years of relevant postdoctoral experience in an academic or pharmaceutical/biotech environment.
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Master's or Ph. D. degree in Pharmacology, Pharmaceutical Sciences, Chemistry, Biochemistry Bioengineering, Biomedical Engineering, or related field. The ARS/AsRS is also responsible for conducting in vitro and in vivo experiments to evaluate the efficacy and safety of novel radiopharmaceuticals in non-clinical models.
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Medical terminology, familiarity with CPT and ICD-10 coding procedures and reference tools, and pharmacology appropriate to the Medical Assistant scope of practice required. Medical terminology, familiarity with CPT and ICD-10 coding procedures and reference tools, and pharmacology appropriate to the Medical Assistant scope of practice required.
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The faculty candidate is encouraged to interact with current Downstate neuroscience researchers in Physiology & Pharmacology, Ophthalmology, Neurology, Psychiatry, and other departments, helping to make the institution more competitive for large collaborative institutional grants.
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Job Description 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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Job Requirements BS degree with 2 years of experience in biology, cell biology, neuroscience, behavioral neuroscience, pharmacology, immunology, or related disciplines is required. Experience in molecular biology (RNA extraction, RT-qPCR, western blot) and cell culture in a BSL2 environment is preferred.
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And respond to regulatory inquiries related to DMPK, PK/PD, and clinical pharmacology. Ensure that appropriate PK, PD and PK/PD data analyses (including population PK, PK/PD modeling and simulation) are conducted for each study/program while adhering to timelines and budgets to insure prompt and accurate execution of deliverables from clinical pharmacology studies and programs.
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4 or More Years of experience in the pharmaceutical industry, regulatory agency or academia, with exposure to drug development, clinical pharmacology, and/or epidemiology required. The individual assuming this role may function as a key member of the Global Product Team in collaboration with Clinical Development, Regulatory, Project Management, Biostatistics, Pharmacology, and other departments to strategically manage benefit-risk throughout the lifecycle of the drug.
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Opportunities to expand to other indications and modalities within genetic medicine GENERAL ROLE DESCRIPTION: The Senior Scientist Pharmacology role will be in the Biomarkers & Immunology group.
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Understanding and application of the pharmacology, chemistry and non-clinical toxicology to effectively conduct safety surveillance. The PST lead will be responsible and provide safety oversight (e.g. surveillance, signal detection, validation, and assessment) for early oncology products with a proactive approach to clinical safety, and will be interpreting regulations related to pharmacovigilance to support all patient safety activities.
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MD / DO with 2+ years of internal medicine residency with patient management experience required; PhD or Clinical Pharmacology fellowship is preferred in addition to MD / DO, not required. MD / DO with 2+ years of internal medicine residency with patient management experience required; PhD or Clinical Pharmacology fellowship is preferred in addition to MD / DO, not required.
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