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A bachelor's degree in toxicology, epidemiology, pharmacology, environmental science, or another related subject. A bachelor's degree in toxicology, epidemiology, pharmacology, environmental science, or another related subject.
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BS/MS in pharmacology, biology or related disciplines. The Senior Research Associate will be a key player in driving genomic medicine pipeline project through target validation, candidate selection and IND-enabling phases using in vitro, in vivo and ex vivo studies.
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Responsible for all areas of preclinical research and development, including generating pharmacology and toxicology data, preclinical trial strategy and design, preparation of the preclinical development plan to support successful INDs, and contribution to regulatory strategy.
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Perform in vivo pharmacology research in a matrixed environment, as well as external academic collaborations and an extensive network of CROs. Perform in-vitro assays; including ELISA, ELISpot, Luminex, flow cytometry, and qPCR.
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Experience in in vivo pharmacology preferred. With advanced gene editing technology, GemPharmatech has created a collection of over 22,000 GEMMs for therapeutic applications such as oncology, metabolic diseases, cardiovascular diseases, pharmacology studies and others.
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The successful candidate will use their strong in vivo pharmacology background and complementary laboratory skills to support discovery efforts and established pipeline projects with an emphasis on anti-obesity therapeutics.
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PhD in pharmacology, immunology, cancer biology, or related field in Biomedical Sciences with a minimum of 3+ years of academic or biotech/pharmaceutical industry experience. Biocytogen Boston in vivo Team is seeking a talented, enthusiastic, highly motivated in vivo Pharmacologist to execute relevant disease models to support preclinical research services for biotech or pharma companies.
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Ampersand is currently seeking an experienced leader with deep expertise in drug development to head our In Vivo Pharmacology team. 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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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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Lead, manage and mentor the in vivo Pharmacology team. Integrate data to provide a detailed understanding of the pharmacology of therapeutic proteins to enable understanding of in vitro MOAs and in vivo correlates of efficacy.
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The successful candidate for this in vivo associate position will have a strong track record in the execution and analysis of in vivo studies, with excellent knowledge in all aspects of in vivo pharmacology.
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BS or MS in biology, biochemistry, pharmacology or related discipline with at least 3-4 years of research experience in an academic or industry setting. Help establish the pharmacology group and contribute to building a culture that embraces continuous learning and improvement.
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The successful candidate will play an integral role across our oncology research groups, overseeing the development of relevant in vivo animal and cell models, and the design and execution of pharmacology studies to propel our pre-clinical research and early development oncology pipeline in addition to Translational initiatives, such as in vivo combination evaluations.
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Murine tumor models and study protocols, ensuring compliance with regulatory, ethical, and quality standards; including serving as Principal Investigator on internal in vivo pharmacology protocols.
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Proficiency in in vivo pharmacology, cell engineering, and genetically engineered mouse models (GEMMs). Utilizing advanced gene editing technology, we have developed an extensive collection of over 22,000 GEMMs, catering to various therapeutic applications such as tumor therapies, metabolic diseases, cardiovascular diseases, and pharmacology studies.
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pharmacology job
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