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The Icosavax preclinical group, based in Seattle, WA is seeking a Director, Vaccines Research with a strong background in vaccine research, antigen discovery and development, and protein biochemistry with prior experience in protein expression, purification and characterization to help progress our vaccine candidates through preclinical pipeline into early clinical development.
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5.0mm SAFE investment in Eleven Therapeutics Ltd., a preclinical-stage company focused on the discovery of RNA interference therapeutics for respiratory disease. $5.0mm convertible debt investment in Cerberus Therapeutics, Inc., a preclinical biotechnology company exploiting single domain antibody fragments to create novel therapeutics for immune modulation.
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This position in the DLMP aligns with unique resources available at the Washington National Primate Research Center (WaNPRC), one of only seven such NIH-supported centers established in 1959 to provide specialized resources and expertise to carry out preclinical and translational research impacting human health.
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The position requires direct management of pharmacology scientists as well as serving as project team leader for 1-2 preclinical stage drug discovery teams. Knowledge of FDA, EMA/ICH regulations and requirements for GLP preclinical study design and documentation.
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The core team leader is accountable for coordinating a matrixed team of subject matter experts working to rapidly progress preclinical therapeutic programs while delivering deeper mechanistic insights into the underlying biology.
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The Clinical Biomarker Lead will be accountable for robust clinical biomarker strategic, operational planning, and execution in support of oncology clinical programs for novel biologic drugs (eg TCE, ADC) starting from preclinical stage through Phase 1/2 clinical trials.
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As a Senior Study Director, you will be responsible for participating in the design of non-clinical / preclinical in vivo studies as well as providing the scientific oversight of the study. Preclinical/ Nonclinical Drug Development.
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Alongside ongoing clinical trials, SystImmune has a strong preclinical pipeline of potential cancer therapeutics in the discovery or IND-enabling stages, representing cutting-edge biologics development.
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In close cooperation with our customers, Bruker is enabling innovation, improved productivity, and customer success in life science molecular research, in applied and pharma applications, in microscopy and nanoanalysis, and in industrial applications, as well as in cell biology, preclinical imaging, clinical phenomics and proteomics research and clinical microbiology.
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The Research and Development group is seeking a Project Manager to work closely with team and project leaders to coordinate the execution of Discovery and Preclinical projects. PhD degree in biology, immunology, biochemistry, virology, biomedical science or related field of study; or equivalent combination of degree and experience.
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Experience with preclinical and clinical regulatory affairs topics. BA/BS degree in molecular biology, cell biology, biochemistry, protein chemistry or similar. The primary responsibilities are to develop and execute global (with an emphasis on US and EU) CMC regulatory strategies towards regulatory adoption of innovative approaches to biologics product and process design, and manufacturing; to lead and manage CMC matters for internal and external products and.
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Extensive oncology experience, including proficiency in target/disease biology, preclinical, and clinical development. Develop and enforce operational standards for biomarker management, vendor relations, and internal processes to ensure program quality, efficiency, and regulatory compliance.
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Consults with Research & Preclinical colleagues on statistical questions in their work. Proficiency in R programming language and other statistical software, including EAST.Experience with CDISC, including SDTM, ADaM, CDASH.Experience in representing sponsors in meetings with interaction with US FDA and international regulatory authorities.
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In doing so, the Program Lead will provide high level oversight, management, and drive across the span of product development from strategy formulation to execution of that strategy; this encompasses the entire process from preclinical research through registration and market entry.
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Certain positions at Bruker require compliance with export control laws and as a result, all interviewed candidates for all positions will be screened pre-interview to determine their eligibility in light of export control restrictions.
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preclinical job in Seattle, WA
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