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The Protocol Project Manager (PPM) will work within a specified oncology disease program and serve as the main point of contact between the study team including faculty and clinical research coordinators (CRC), outside entities such as sponsors, and various departments within UCSF providing support.
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Education: Bachelor's degree in Chemistry, Biochemistry, Biology, Microbiology, Molecular Biology, or Analytics. Assay Development and Execution: Thoughtfully design, construct, and meticulously test techniques to refine the structural and functional attributes of protein products.
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Adapt data science algorithms (supervised and unsupervised learning, decision trees, neural networks, AI based image processing and feature extraction, Bayesian learning, etc) for modeling clinical trial data to support drug development Responsible for planning and implementation of analyses to integrate knowledge of pharmacokinetics, pharmacodynamics, patient characteristics and disease states to optimize doses, dosage regimens and study designs.
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Founded in 2015, the company has built a portfolio of 30+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
$205,000 - $260,000 a yearFull-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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The Translational Medicine department at Genentech informs clinical development of Client personalized therapeutics through establishment of biomarker strategies aimed to study biological pathways driving disease and by characterizing the mechanism of action of Client therapeutics.
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Advanced degree (Ph. D. preferred) in biology, biotechnology, biochemistry, cellular/molecular biology, molecular genetics, microbiology or related degree. Our client is a major Am law 100 firm, seeking a Patent Agent for all offices, including Chicago; Atlanta; Boston; DC; Denver; Dallas, Houston; Fort Lauderdale; Miami; Nashville; New York; Phoenix; Raleigh; Salt Lake City; Del Mar, Los Angeles, Palo Alto, San Diego, San Francisco; Seattle; St. Louis; Wilmington.
$110,000 - $180,000 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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The company's conditionally activated siRNA (CASi) platform integrates RNA nanotechnology with RNA medicinal chemistry to create siRNA pro-drugs that can activate or suppress their own drug activities based on the presence or absence of disease indicating RNA markers in mammalian cells.
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CERTIFICATION & LICENSURE: Certified Clinical Documentation Specialist (CCDS) or Certified Documentation Improvement Practitioner (CDIP)Certified Coding Specialist (CCS) or Certified Professional Coder (CPC)SKILLS AND KNOWLEDGE:Knowledge of Pathophysiology and Disease Processes sufficient to pass the clinical pre-employment test at a rate of 85% or better is required for new hires.
$63.74 - $95.6 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Immunology, Cardiovascular, Fibrosis, and Neurology (ICFN) Translational Medicine Disease Team drives the strategy for the multiple disease areas of interest, including Rheumatology, Dermatology, Gastroenterology, Neuroscience, Heart Failure, Thrombosis, and Lung Fibrosis.
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Our comprehensive platform includes non-invasive monitoring devices, clinical software, and decision support tools, such as the revolutionary Eko Core Digital Stethoscope, recognized as a TIME Magazine “Best Invention of the Year.” Our latest FDcleared DUO device combines a digital stethoscope with an ECG cardiac monitor and AI, providing seamless in-clinic and at-home monitoring for 28 million heart disease patients.
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Founded in 2015, the company has built a portfolio of 20+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
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The ideal candidate should hold an advanced degree (Ph. D. preferred) in biology, biotechnology, biochemistry, cellular/molecular biology, molecular genetics, microbiology, or a comparable field.
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In close cooperation with our customers, Bruker is enabling innovation, improved productivity, and customer success in life science molecular research, in applied and pharma applications, in microscopy and nanoanalysis, and in industrial applications, as well as in cell biology, preclinical imaging, clinical phenomics and proteomics research and clinical microbiology.
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Kyverna is recruiting a highly motivated Senior Scientist, Formulation Development in its Technical Operations organization to help advance its mission to free patients from the siege of autoimmune disease.
$140,000 - $185,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Patients can be admitted for diagnostic work-ups, treatment of infectious disease processes, palliative care and end of life care. Patients can be admitted for diagnostic work-ups, treatment of infectious disease processes, palliative care and end of life care.
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disease infectious microbiology jobs Title: post Company: Emory University in San Francisco, CA
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