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In this position, you will assist with the design and execution of in vivo pharmacology experiments in rodents. Investigate and validate mechanism of action of drug leads by conducting in vivo, ex vivo and in vitro pharmacology experiments.
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Caribou Biosciences is a leading clinical-stage CRISPR genome-editing biopharmaceutical company dedicated to developing transformative therapies for patients with devastating diseases. Design and implement multi-color flow cytometry panels for cell phenotyping.
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The current role is for a Senior Research Associate, Translational Sciences - to join our in-vivo pharmacology team. A BS/BA in Biology, or closely related field with 10+ years of lab experience in in-vivo pharmacology and/or bioanalysis in pharmaceutical environments.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The ideal candidate will have a blend of broad experience that spans chemistry, biochemistry, proteomics, and biopharmaceutical production. Work Experience: 5 or more years' experience in chromatography focused applications within the biopharmaceutical segment is ideal.
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We are actively seeking a senior patent attorney or patent agent with an advanced degree, preferably a Ph. D., in a life-science field, such as biology, molecular biology, biochemistry, pharmacology, or immunology, and at least 5 years of experience in preparing and prosecuting patent applications.
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Coordinate closely with cross-functional teams including Quality Control, Bioinformatics, Translational, Analytical Development, Supply Chain, Process Development, and Manufacturing to ensure seamless sample management.
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The Department's 17 divisions include Academic General Pediatrics, Child Development& Community Health; Allergy, Immunology and Rheumatology; Cardiology; Environmental Science & Health; Emergency Medicine; Endocrinology; Gastroenterology; Genetics; Genome Information Sciences; Hematology/Oncology; Hospital Medicine; Infectious Diseases; Neonatology; Nephrology; Pharmacology & Drug Discovery; Rehabilitation Medicine; and Respiratory Medicine.
RemoteExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Caribou is looking for a Senior Patent Administrator to provide full support to the in-house Director of Intellectual Property and Chief Legal Officer on all intellectual property matters. Review and process all incoming patent-related correspondence from USPTO, WIPO, and foreign counsel; run docketing and status reports for Director of Intellectual Property, Chief Legal Officer, and Finance Department.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Pacific BioLabs is an independent CRO offering cGMP/GLP testing services in toxicology, biocompatibility, pharmacology, analytical chemistry, and microbiology. Pacific BioLabs is an independent CRO offering cGMP/GLP testing services in toxicology, biocompatibility, pharmacology, analytical chemistry, and microbiology.
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At least 5 years of experience as an attorney in a law firm or in-house legal department, with a focus on providing transactional and regulatory advice regarding marketed products in the biopharmaceutical or biotechnology industry.
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Reporting to the Senior Director of Regulatory Operations, you will be responsible for assembling, formatting, and publishing regulatory dossiers (e.g., IND, CTA, BLA, MAA) for global registration and lifecycle management submissions (e.g., supplements, amendments, variations) to meet corporate objectives for both ongoing business and new product development.
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Bachelor's degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields. as part of the Regulatory Affairs Asia Pacific (APAC) team, on-site at our Diabetes Care Division HQ location in Alameda, CA. As an individual contributor, the function of a Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment.
$65,900 - $131,900 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Knowledge of capillary electrophoresis (CE) and mass spectrometry (MS) in the biopharmaceutical, biotech, or life science industries and previous product management experience. No less than 7 + years of experience in Biopharma, Biotech or Life Science product management, marketing, sales, or application scientist roles.
Full-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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This Senior International Regulatory Operations Specialist will work on-site at our Alameda, CA location in the Diabetes Care Division. 2-3 years of experience in regulatory preferred but may consider quality assurance, research and development/support, engineering, scientific affairs, operations, or related area.
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Experience in the biotechnology and biopharmaceutical industry is preferred. We currently have a suite of products that allow for rapid, stable instrument deployment and are poised to make headway into clinical markets with controls for engineered cell therapies.
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pharmacology biopharmaceutical jobs in Berkeley, CA
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