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Proven track record of leading successful peptide drug discovery programs, resulting in the advancement of drug candidates into preclinical or clinical stages. Work closely with the regulatory affairs team to ensure that all peptide drug discovery activities adhere to relevant regulatory guidelines and requirements.
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This position is part of the Warren Center for Neuroscience Drug Discovery (WCNDD) at Vanderbilt University where traditional academic pursuits in basic science are extended to advance our understanding of human disease and drug targets to directly impact patient care.
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And minimum 7 years global Drug Safety/Pharmacovigilance clinical trial and post marketing experience in a pharmaceutical or biotechnology industry in positions of increasing technical and leadership responsibility.
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Alpha Bio is an early-stage and rapidly growing drug discovery company headquartered in Seattle, WA. We are enabling the next generation of high-impact therapeutics by combining high-throughput synthetic biology to measure protein-protein interactions at scale with state-of-the-art machine learning to predict how proteins bind.
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This role is a great opportunity to join the fast-growing field of Induced Protein Proximity applied to drug discovery. The postdoc will apply NMR spectroscopy to create novel methodologies for the discovery and development of molecular glue molecules, taking a multi-disciplinary approach that combines computational methods and experimental techniques.
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Open Rank of UNMCCC IM Molecular Medicine - Target & Drug Discovery (Cancer Therapeutics) Researcher
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Successful applicants will have a strong track record of scientific accomplishments in the identification of new cancer targets and/or drug discovery and development exemplified by peer-reviewed (NCI, NIH, or other agencies) or industry funding, high quality publications, and collaborative research.
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We are currently seeking a National Accounts Manager - Drug Channel reporting to the Team Lead for Small Format. BlueTriton Brands, Inc. ("BlueTriton") is a water and beverage company in North America that produces and distributes a portfolio of brands of spring water, purified water, and other beverages, which include Poland Spring®, Deer Park®, Ozarka®, Ice Mountain®, Zephyrhills®, Arrowhead®, Origin™, Saratoga®, AC+ION®, Pure Life®, B'EAU®, and Splash Refresher.
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Reporting to the Senior Director, Head of Toxicology, Safety Assessment, we are seeking a highly experienced Principal Investigator to lead Discovery/IND/Post-IND stage small molecule drug discovery programs, serving as the nonclinical Safety Assessment lead for multiple programs.
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Drive translational research and development efforts by conducting experiments alongside R&D Scientists in the drug discovery department. Conduct a wide range of biochemistry, molecular and cellular biology techniques to express, purify and characterize drug candidates (e.g. DNA/RNA isolation, plasmid construction, PCR, Octet, HPLC, mammalian cell culture, transient and stable transfections.
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Mandatory drug testing prior to employment and will be subject to random, unannounced drug and/or alcohol testing during employment." Must be a Certified Juvenile Probation Officer, within six months of hire, and a Licensed Chemical Dependency Counselor (LCDC) preferred.
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Firm Type: Law Firm, Experience: 10 Years, Job Title: FDA Drug/Biologics Regulation CounselLocation: New York City, NYOverview: Alaw firm is seeking an experienced FDA Drug/Biologics Regulation Counsel with over 10 years of industry experience in drug and biologics development.
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Demonstrated expertise in AI-driven drug discovery, machine and deep learning, computational biology, or bioinformatics research. Leading the development and optimization of the AI algorithms for protein- and RNtargeted drug discovery.
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Oversight and review of drug safety operations practices. Ensure case reports are appropriately scheduled in Argus based on regulatory reporting matrix in conjunction with Drug Safety submissions.
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This role is responsible for overseeing all aspects of drug safety study operational activities from study start up to close out. Develop and/or update SOPs, processes and practices for SAE and other safety data collection in accordance with drug safety and pharmacovigilance regulations, ICH standards and guidelines as appropriate to ensure timely and compliance submissions to worldwide regulatory agencies.
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TScan’s discovery platform is centered around a breakthrough technology that enables the rapid, comprehensive, and genome-wide identification of the peptide antigen targets of T cell receptors.
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Title: drug discovery Company: Vc Backed Newco
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