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Have a thorough understanding of concepts in toxicology and pharmacology including in vivo, in vitro, and in silico test methods and familiarity with the laws, regulations, and practices related to toxicological testing.
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Previous patent prosecution law firm experience, patent bar membership, and a background in one of the following fields: cell or molecular biology, immunology, biochemistry, bioinformatics, organic chemistry, medicinal chemistry, cancer biology, pharmacology.
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Successful completion of an American Academy of Professional Coders (AAPC) American Health Information Management Association (AHIMA) coding certification preparation course for professional services or facility coding that includes medical terminology, anatomy and physiology, health information management concepts, and pharmacology.
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The Program Leader will lead a cross-functional team across clinical operations, regulatory affairs, clinical pharmacology, biomarkers, CMC, non-clinical, and medical to deliver against the program strategy.
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Publish and present research findings within the community of bioorganic chemistry, synthetic organic chemistry, and pharmacology. This position requires strong collaboration skills to ensure timely completion of research projects and effective communication within the bioorganic chemistry, synthetic organic chemistry, and pharmacology communities.
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The candidate should possess an advanced degree in biochemistry, microbiology, molecular biology, organic chemistry, pharmacology, or a related field. Our ideal candidate is an experienced patent agent that can help us build and expand our chemical and biotechnology patent prosecution practice.
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While its historical focus has been radioprotection and parasitic disease, ET applies its core competencies of medicinal, synthetic, and analytical chemistry as well as clinical pharmacology to all therapeutic areas within the Medical Research and Development Command's portfolio.
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A Master's or Ph. D. in a scientific field such as toxicology, pharmacology, genetics, immunology, epidemiology, molecular biology, cell biology, pathology, chemistry, environmental health, or related life sciences and a minimum of 3 years of experience in project management, drug or chemical safety evaluation, scientific consulting, and/or regulatory affairs.
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We are currently seeking a FIFRA Regulatory Toxicologist for a Manager level position in our Chemical Regulation and Food Safety Practice in Washington, DC. Other locations maybe considered. Ph. D. in Toxicology, Pharmacology, or a related discipline; Masters degree also considered.
$110,000 - $155,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Knowledge of medical ethics, human anatomy, pharmacology, and other specialties. Our core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS programs.
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Experience in Biology, Molecular Biology, Physiology, Pharmacology, Biomedical Engineering, Nuclear, Industrial Radiology, or Biological Technologies. Carry out molecular biological experiments, including cell culture, tissue homogenization, protein and RNA extraction techniques, multiplex enzyme-linked immunosorbent assay, Western blotting, RT-PCR, tissue handling and flow cytometry.
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The LVT must possess a broad knowledge of animal science, medicine, and husbandry, including a basic knowledge of pharmacology and sufficient mathematical skills to ensure the administration of the accurate drug and fluid doses.
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Knowledge of pharmacology of various drugs and their therapeutic and adverse actions and complications. PACU, Ambulatory Surgery Center, Pre-Op and Perioperative Care. HRSA Loan Forgiveness available.
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4-year degree or equivalent preferably within Biology, Pharmacology, or a health-related field. This is a full-time on-site role for a Clinical Research Coordinator. The Clinical Research Coordinator will be responsible for managing clinical research studies, ensuring protocol compliance, obtaining informed consent from study participants, and coordinating with study sponsors and regulatory agencies.
$47,000 - $60,000 a yearFull-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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Ph. D. in toxicology, biology/pharmacology, with at least 10 years related experience with vaccines and other biologics. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries.
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toxicologist pharmacology jobs in Washington, DC
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