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Lead drug substance team through preclinical and clinical development to commercialization across Astria’s pipeline. This role will oversee all drug substance process development for the company and will play a key role in driving the portfolio forward from early process development through late stage, including process characterization, validation, and commercialization.
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The Associate Director/Director Upstream Process Development and Technical Operations will be directly responsible for the process development and technical manufacturing elements of AVEO’s biologics drug substance programs.
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Drug discovery knowledge, biopharma CRO and relevant business experience required. GemPharmatech is a global company providing high-quality products and model systems for preclinical discovery, testing, and development of new drugs and therapeutic solutions.
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The Vice President of Business Development will engage with pharmaceutical companies and hospitals to commercialize Pear Bio’s precision medicine platform and drug discovery pipeline. You will build connections with medium-large pharmaceutical companies to explore partnership structures for the various applications of the Pear Bio technology, including target identification, drug discovery/development, translational studies, patient stratification and companion diagnostics development.
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Ph. D. with minimum of 15 years of working experience, including proven track record in the discovery and development of drugs for diseases of peripheral tissues/organs in the pharmaceutical and/or biotechnology industry, substantiated by publications, patent filings, and/or other, from tenure in drug discovery and development as characterized.
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Direct the execution of multiple early drug discovery programs, including setting scientific direction, development of program timelines, monitoring of key milestones and decision points, and managing scientific team.
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Studies will include rat and mouse biodistribution, disease model development, drug efficacy, and toxicology-like studies in neurology, oncology, and other therapeutic areas. Overview:The In vivo Associate Scientist II position will execute in vivo support for pre-clinical biomedical imaging and pathology studies toward pharmaceutical discovery and development.
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Domain expertise in rare disease drug development and trial recruitment. This impactful role is an opportunity to build a function, shape the development of Ensoma's in vivo therapies, and ultimately enable a better future for patients.
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We are seeking a skilled, motivated, and versatile individual who can help build a highly collaborative, successful drug discovery and development team in the Obesity Research group in Cambridge.
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Ampersand is currently seeking an experienced leader with deep expertise in drug development to head our In Vivo Pharmacology team. Deep understanding of the role of translational research/medicine in drug development.
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Plan and independently implement in vivo studies and in vivo assay development and optimization to support preclinical characterization and evaluation of targets/pathways that regulate energy balance.
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The Company’s mission is to discover, develop, and commercialize transformative oncology therapies for patients, while leading the advancement of AI-driven structural ensemble and computational drug design.
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Ensuring leadership and oversight for development and implementation of in vivo preclinical efficacy, safety and PK/PD studies. The ability to collaborate closely with the leadership team and other R&D leaders while guiding the in vivo pharmacology team to achieve the company's objectives is an essential element of the role.
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Founded in 2017 and based in Chicago, Meitheal Pharmaceuticals is focused on the development and commercialization of generic injectables and, as of 2022, has expanded its focus to include fertility, biologics, and biosimilars.
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Affini-T Therapeutics is announcing a Senior Director, Head of Product Sciences opportunity at our headquarters in Watertown, MA. Position Summary The Head of Product Sciences role is situated within the larger CMC organization responsible for process development, analytical development, technology transfers, manufacturing, and supply of our drug product TCR T cell candidates, drug substance and critical intermediates such as gene editing reagents, viral (LVV) and non-viral vectors.
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