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IDEAYA Biosciences (NASDAQ: IDYA) is a public, clinical-stage precision medicine oncology company committed to the discovery and development of targeted therapeutics for patient populations selected using DNA sequencing and other molecular diagnostics.
$315,700 - $348,100 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Responsible for leading all clinical pharmacology activities in support of Inmagene development programs, bridging between preclinical and clinical activities, and supporting early, as well as late-stage, clinical programs.
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Analyze and interpret a wide range of information (including clinical and preclinical data, scientific literature, and diverse expert views) to form independent viewpoints. The analyst will independently conduct due diligence on healthcare companies and proactively generate bottom-up investment ideas, primarily in public equity investments and selectively in private early-stage investments.
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Experience working with other functions including preclinical and late-stage clinical development and external collaborators. Keywords : MD, medical doctor, consultant, medical monitor, early clinical development, oncology, cancer, solid tumors, small molecules, targeted therapy, clinical trial, study, protocol, asset, pharma, biotech, biopharma, MD, phase I, first-in-human, FIH, IND, phase II, FDA.
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Ovid Therapeutics is seeking an experienced Program Manager to work with cross-functional teams and enable execution of preclinical and clinical stage programs aimed at meaningfully improving the lives of patients and families affected by epilepsies and other brain disorders.
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Currently celebrating our 22 nd anniversary, we have a strong pipeline with projects in preclinical development stage through Phase III. We celebrate science, welcome curiosity, expect collaboration and demand integrity and respect in all we do, create and deliver.
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MS in Pharmacokinetics, Pharmaceutical Sciences, Pharmacology, Chemistry, Biochemistry, or related field with a specific focus on PK and PK/PD modeling and simulation and 10+ years of Pharmaceutical/Biotech industry experience in conduct and/or oversight of late-stage Modeling and Simulation activities, including conduct or oversight of small molecule population pharmacokinetic analyses.
$125,700 - $182,250 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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You will be responsible for oversight and interaction with consultants and CROs assigned to support clinical pharmacology tasks including preclinical PK, modeling, and clinical assay development.
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This position will partner with functional sub-team leaders to lead project management activities for a cell therapy program sub-team, guiding the sub-team through preclinical and clinical development.
$145,000 - $175,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Amplify Bio is a leading contract research organization with a comprehensive range of services that span from being an outsourcing partner for discovery stage R&D work, a preclinical CRO performing safety efficacy and toxicology studies for small molecules and advanced therapies alike, and, most recently, an expansion into manufacturing services for cell, gene, and mRNbased therapeutics.
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Drive planning for key drug development stage-gate decision points after Phase 1 and co-chair stage-gate committee for Rare Disease franchise. Successful candidate will have a strong understanding of the drug development process from preclinical pharmacology through to regulatory approval and the principles, concepts, practices, and standards of pharmaceutical program management.
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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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In addition to a set of advanced programs in the clinic, they have a deep pipeline of wholly owned preclinical candidates, as well as productive collaborations with Merck, AbbVie, Gilead and Bristol Myers Squibb in a broad range of disease areas.
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ArsenalBio, a privately held, clinical-stage programmable cell therapy company engineering advanced CAR T therapies for solid tumors, is seeking a talented Associate Director, Cell Line Development to work onsite based in our South San Francisco office.
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Experience and familiarity in the CMC regulatory environment for early to mid-stage development. Experience in a virtual biotech setting working with external CDMO and CRO based resources for preclinical activities, production of drug substance and drug product, testing, and CTM labeling is a plus.
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