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Act as a technology expert and scientific liaison for several external research partnerships of high strategic importance to BMS. Lead the biology team for one of BMS' small molecule drug discovery programs.
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With a strong mission, this firm are having a genuine impact on the future of drug development. They are the first company to bring to market their breakthrough in biology discovery. You will also play a hands-on technical role in a hybrid capacity working across their cloud computing and networking environment.
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Over forty biotech companies are using our platform to accelerate their ability to engineer biology, from drug discovery to bioproduction. Over forty biotech companies are using our platform to accelerate their ability to engineer biology, from drug discovery to bioproduction.
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Develop applications with customers and ensure customer success in the context of our target markets (e.g. genomics and drug discovery) Knowledge of drug discovery and genomics workflows is strongly preferred.
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Bachelor’s with 5+ years or MS / PhD with 1+ years in a medically-related field with a quantitative focus (public health, health economics, biostatistics) or in in a quantitative field (computer science, statistics, computational biology, biomedical engineering.
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GenScript ProBio is the subsidiary of GenScript Biotech Corporation, proactively providing end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy (CGT), vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers.
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BS/BA degree in a relevant scientific discipline or MSc in Biology, Life Science, or related field. The team is involved in developing regulatory product strategies for the Immunology and Inflammation therapeutic area, leading regulatory efforts in the development stage of drug products.
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Master's Degree in Life Science, Pharmacology, Toxicology, Biology, Physics, or similar analytical science field or Bachelor of Science in similar field with 1 year of related experience. An advanced understanding of drug metabolism, toxicology, forensic testing, P450 enzymes, or testing principles specifically related to urine and oral fluid metabolism.
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MS/PharmD/PhD in Chemistry, Biology, Biochemistry, business, or related healthcare area. Sound knowledge of drug development and understanding of FDA and ICH GCP guidelines. Prefer experience within preclinical stage *ophthalmic, otic, and/or neurology.
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Act as the lead clinical pharmacologist on clinical pharmacology study teams to support clinical development: independently lead the design, protocol development, execution, analysis, and reporting of clinical pharmacology studies (e.g., food effect, BA/BE, human ADME, drug interactions, renal and hepatic impairment, etc.
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Bachelors degree in Geology, Hydrology, Civil, Chemical or Environmental Engineering, Chemistry, Biology, or other Natural Science. All employees must pass Non-DOT pre-employment drug screening and follow all UIC Non-DOT Drug and Alcohol Testing Program guidelines and requirements.
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Our preclinical pipeline extends beyond to biologics against novel immuno-oncology targets, antibody-drug conjugates, bispecific and trispecific antibodies, and small molecules expected to reach the clinic in 6-24 months, underscoring our bench-to-bedside approach.
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Champion novel technology platforms (build, expand and improve capabilities) to solidify Incyte's position as an Innovative leader in the industry · Set strategy for immunology research areas and maintain strategic focus across multiple complex drug discovery programs in prioritizing resource allocation and drive decisions consistent with corporate goals.
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The successful candidate will join a dynamic, multi-disciplinary team of scientists in exploratory immuno-oncology, playing a key role in the evaluation and understanding of new drug concepts in vitro and in vivo.
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Preferred: PMP or CAPM or similar project management certification or equivalent experience. Working knowledge of relevant therapeutic areas and experience working within development of preclinical through translational stage clinical studies.
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