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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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Assistance with preclinical studies. Bachelor's or Associate's degree in one of the Life Sciences or Engineering disciplines including Biomedical Engineering, Cell Biology, or Tissue Engineering.
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This is a great opportunity to work cross-functionally and get exposure to products in a preclinical setting. Demonstrated experience in PCB design - Altium. Some responsibilities include leading a technical team of engineers and technicians, developing hardware DMFEAs, PCB design, prototyping, evaluating electrical components, assessing and testing to safety standards, mentoring junior engineers and technicians etc.
$120,000 - $135,001 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Offering expert guidance from concept-through-commercialization, including product design and engineering, preclinical and clinical development, data management, market access, regulatory affairs and quality assurance, Veranex enables accelerated speed to market, controlled development costs, development risk mitigation, and accelerated market viability assessment.
Full-timeRemoteExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Plans and executes laboratory, preclinical or clinical research to prove feasibility of concepts. Knowledge of sensor technologies and diagnostic/monitoring solutions for chronic diseases, especially in the cardiac spaceKnowledge of statistics and advanced signal processing techniques (e.g. time frequency analysis, statistical signal processing, adaptive signal processing)Proficiency in MATLAB, Python or other scripting languageKnowledge of human physiologyTeam player with good communication skills - written, verbal, and interpersonalQuality System Requirements.
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You have experience supporting preclinical animal and cadaver evaluations and the desire to lead them. You are detail oriented and able to provide thorough reviews and authorship of preclinical protocols and reports.
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Bachelor’s degree in industrial design, user experience design, anthropology, human factors engineering, biomedical engineering, or related field. The Principal Design Researcher leads generative and evaluative research projects across a spectrum of disease states and medical device challenges.
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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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Serves as the Study Director for GLP and non-GLP preclinical studies and assures that all applicable GLP regulations are followed. Serves as the Study Director for GLP and non-GLP preclinical studies and assures that all applicable GLP regulations are followed.
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The role will report to Director of Preclinical and Toxicology assessment team responsible drugs and devices for Peritoneal dialysis, Hemodialysis, and Acute therapies ($5B product portfolio with global reach in more than 100 countries.
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Your Role: The Associate Director of Preclinical (Toxicology and biocompatibility) will support a portfolio of drug, medical device, drug packaging system, and/or combination product development and global registration.
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Assists with administrative support for DoS faculty outside of the Preclinical Research Center on an as needed basis. The Department of Surgery's Preclinical Research Center seeks a motivated Research Professional 1.
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Participate in project team development activities by designing and executing exploratory bench, animal and cadaver studies to test vascular devices and support the design and development phase. You have a Bachelor of Science in Engineering discipline (Mechanical, Materials Science, Biomechanical, Bioengineering, Biomedical) required.
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Experience with Omni-Assistant QMS Software and Good Laboratory Practice. Assists with maintaining the Omni-Assistant QMS document portfolio for the program. Assists with maintaining the Omni-Assistant QMS document portfolio for the program.
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As a premier Contract Research, Development, and Manufacturing Organization (CRDMO), WuXi STA offers its worldwide partners efficient, flexible and high-quality solutions for integrated chemical, manufacturing and controls (CMC) from preclinical to commercial uses.
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preclinical job in Minneapolis, MN
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