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Expert understanding of global clinical study design and drug development process from discovery to registration and post-marketing. MD, PharmD. or PhD. within a clinical and/or scientific profession (or an equivalent level of professional, clinical and/or scientific education, training and experience) required.
$168,800 - $228,800 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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We are expanding our capabilities in informatics across multiple drug discovery platforms, including DNencoded library (DEL) screening, peptide-display discovery, support for RNbased therapeutics, parallel medicinal chemistry (PMC), targeted protein degradation, and high-throughput screening (HTS.
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Relationships This role reports to the Senior Scientific Director of SMDC. They will have close interactions with scientists and experts within Computational Drug Discovery, Medicinal Chemistry, Quantitative Biology and ADME & Tox. Additional internal partners include data scientists, data engineers, ML specialists, software developers and others across US, UK, and Denmark.
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Participate in cutting-edge research in machine learning and methods development for scientific discovery, including large language models and drug discovery. gCS Prescient Design is seeking an exceptional Staff Machine Learning Engineer to develop our LLM and AI product and enable the next generation of foundational research in machine learning for scientific discovery.
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We are seeking a highly motivated and experienced Associate Director Regulatory Affairs with expertise in hematology / oncology to join our Drug Discovery and Early Development team. The right candidate should be comfortable driving IND preparation, IMPD development; CTR compliant CTA applications (initial submissions and maintenance); managing health authority interactions (such as scientific advice meetings); orphan drug designation (ODD) submissions to the FDA and the EMA; and advising teams on asset strategy; indication strategy; clinical study designs and regulatory plans.
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Experience with AAV gene therapy drug development, bench to bedside and with biologics drug discovery and development. Scientific experience in biopharma neuroscience Research and Development with working knowledge across multiple phases of development (pre-IND, Phase 1-3.
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The Therapeutics Discovery organization within Johnson & Johnson is continuing to build key scientific expertise in computational and medicinal chemistry, screening, and pharmacology to partner closely with our outstanding therapeutic area scientists to develop groundbreaking new medicines in the areas of Oncology, Immunology, Neuroscience, Cardiovascular, and Retina.
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Supporting Pfizer Oncology, you will be a senior scientific and strategic leader and a member of the Pharmacometrics and Systems Pharmacology Leadership Team. In this key role, you will influence the discovery and development of drugs and expand the application of model-informed drug development (MIDD) approaches within oncology and across our portfolio.
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The Therapeutics Discovery organization within Janssen R&D is continuing to build key scientific expertise in computational and medicinal chemistry, screening, and pharmacology to partner closely with our outstanding therapeutic area scientists to develop groundbreaking new medicines in the areas of Oncology, Immunology, Neuroscience, Cardiovascular, and Retina.
$131,000 - $225,400 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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We provide efficient scientific and regulatory consulting services throughout the full product lifecycle from molecular discovery to FDA approval & full commercialization to product retirement and generic intrusion.
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We are seeking creative, self-motivated informatics and data scientists to join our In Silico Discovery (ISD) team to bring their expertise to exciting efforts in drug design across both small molecule and alternative modalities.
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As a leader in pharmacy education, scientific discovery, patient care, and community engagement; the school conducts cutting-edge research and engages in a wide variety of professional practice activities to improve the health and well-being of citizens in the state of Maryland and beyond.
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Bachelor's degree or advanced degree (i.e., Masters, PhD ), in a scientific discipline relevant to drug discovery, development, pharmacy, biology, or chemistry and a minimum 10+ years' experience in pharmaceutical or medical device manufacturing Quality Assurance with at least 3 of the years' relevant to parenteral product production and/or device manufacturing.
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Directly related clinical trial experience or experience in areas relevant to drug discovery or development, e.g. epidemiology, toxicology, pharmacovigilance, regulatory affairs. Combined with a minimum of 1 year experience in a related scientific field, e.g. pharmacology, physiology, microbiology.
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Proven track record of scientific leadership and accomplishments in biotechnology, with significant experience in drug discovery and development. The CSO will play a pivotal role in driving our client's scientific strategy, shaping their pipeline of plasma-based therapies, and advancing the understanding of age-related diseases.
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