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Preference for MD/DO and 4+ years of clinical or biotech/pharma industry experience with a proven success record in clinical research studies, trial design, execution and oversight PharmD or PhD in clinical research or clinical pharmacology with 8+ years' scientific and/or drug development experience in the biopharma industry, healthcare, consulting, academia or a related environment.
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The Research Scientist will be involved directly with the development and execution of clinical and preclinical research goals/activities of CRF. The candidate will work under the direction of the facility manager with respect to the department’s radiochemistry program needs, including routine and novel radiotracer development, production, troubleshooting, and prioritization/facilitation of clinical radiotracer translation.
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Leverage close collaborations with quantitative functions within CDS (e.g., Biostatistics, Bioinformatics), as well as in Clinical Research, Patient Safety, Medical Affairs, and Global Value and Access to anticipate and meet the evidence needs of regulators, payers, providers, and patients.
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Strong experience working as or for the Chief Financial Officer in a National Laboratory, Federally Funded Research and Development Center (FFRDC), University or other "not for profit" scientific or research institution and background with funding from the federal government.
$250,000 - $283,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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We are looking for an experienced Regulatory Affairs & Quality Assurance Lead to oversee our Mark I whole-body scanner regulatory submission and maintain market authorisation for our Gemini digital twin platform for compliance and commercial viability.
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Possesses a passion for being part of the scientific and engineering community, helping bring cutting edge research to enable commercial processes. Codexis, a biotechnology company based in Redwood City, CA, is looking to hire a Research Associate III – Protein Engineering.
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We are seeking a driven, creative, collaborative, and highly respected individual who is passionate about public policy, government affairs, regulatory policy, helping patients, innovative science, biotechnology, and public health to serve as Vice President, Policy & Advocacy.
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Deep scientific knowledge and technical skills in de novo binder generation, antibody/protein engineering, protein expression, characterization, and analysis. Key role in aligning the strategic direction for biologics drug discovery in close collaboration with the Thematic Research Centers (TRCs.
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Our incredibly talented team of engineers, innovators, and industry leaders bring years of experience from the top healthcare companies in the world, including: Intuitive, Auris, Stryker, Johnson & Johnson, Boston Scientific, Verb Surgical, Mako, Think Surgical, Medrobotics, and Hansen.
$230,000 - $300,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Stanford ME/CFS Collaborative Research Center operates under the auspices of the Stanford Genome Technology Center (SGTC) and the Stanford School of Medicine. Bachelor's degree in related scientific field and four years of relevant work experience; or Master’s degree in a related scientific field and two years relevant experience; or PhD in related science field.
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Our team is comprised of exceptional engineers, innovators, and industry leaders with extensive experience from top healthcare companies such as Intuitive, Auris, Stryker, Johnson & Johnson, Boston Scientific, Verb Surgical, Mako, Think Surgical, Medrobotics, and Hansen.
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Research-oriented software engineering skills, including fluency with libraries for scientific computing (e.g. SciPy ecosystem) and machine learning (e.g., PyTorch, TensorFlow, Scikit-learn, Pandas.
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Senior Clinical Research Associate. This role of Senior Research Associate for the Analytical Development (AD) position will be responsible for the execution of routine testing, including but not limited to flow cytometry assays used to characterize or release engineered CAR-T cell drug products.
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Existing collaborations within CZ Biohub: Technology Platforms (Bioengineering, Computational Microscopy, Data Science, Genomic Sequencing, Mass Spectrometry/Proteomics), and Research Group Leaders.
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The Director/Sr Regulatory Affairs will lead the overall CMC Regulatory strategy for Adverum’s gene therapy program/s. Manage the Regulatory Affairs (CMC) Strategy for Regulatory Affairs.
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clinical research scientific affairs jobs Title: director Company: Regeneron Pharmaceuticals Inc in Foster City, CA
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