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Top biopharma sponsors, clinical research organizations, healthcare providers and institutions rely on ConcertAI’s evidence-generation and digital transformation capabilities to advance precision medicine and medical innovation.
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Verily’s Clinical Studies Platform (CSP) business is focused on transforming evidence generation within clinical research. 8+ years of clinical study management experience in registries, observational research, RWD/E, or clinical trials as a clinical study lead/project manager.
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Nola Hylton, PhD (Professor, Department of Radiology and Biomedical Imaging, Director, Breast Imaging Research Program, University of California, San Francisco) Knowledge in breast imaging acquisition methods (MRI, mammography, ultrasound and/or PET) and clinical trials is highly desirable.
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Translational research is carried out every day in the hundreds of clinical trials of promising new therapies offered through UC San Diego Health, and in the drive of our researchers and clinician-scientists who are committed to having a significant impact on patient care.
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The candidate will work collaboratively with faculty within the Department of Radiology and Biomedical Imaging and other departments at UCSF to advance the development of new molecular imaging agents, from early tracer development to first-in-man clinical studies.
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OCTA services improve compliance and enable a more rapid activation of clinical trials to increase and improve patient care and provide cutting edge treatment opportunities for our patients and advance our research mission.
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The scientific mission of the DEB is to perform outstanding basic, clinical, and population health research along a spectrum from molecules to society and to develop tools for the translation of knowledge that will improve clinical practice and population health and ensure optimal use of resources.
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Its mission is to improve the health and well-being of all people through medical research and education in neuroscience, cardiovascular biology, immunology, and stem cell biology. Willingness and ability to learn new methods and skills for changing research priorities.
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Licensed (or licensed eligible) by the Board of Behavioral Science in California as a Marriage and Family Therapist, Licensed Clinical Social Worker or Licensed Professional Clinical Counselor.
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This is on onsite opportunity in Alameda, CA.What You'll DoEnsure alignment of key internal stakeholders (commercial, RWE, medical and clinical teams) on business priorities and Health Economics & Outcomes Research / market access projects.
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The Quantitative Biosciences Institute (QBI) is an Organized Research Unit (ORU) at UCSF that seeks transformative results in biomedicine; QBI supports fundamental quantitative research in the biological sciences.
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Strong knowledge of model-informed drug development, DMPK-Clinical Pharmacology concepts, and regulatory requirements. A Ph. D. or PharmD with a minimum of 10 years of industry experience in pharmaceutical sciences, pharmacokinetics, clinical pharmacology, chemistry, or related fields.
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Strong knowledge of pharmacokinetics and modeling, pharmacodynamic principles, ADME concepts, bioanalytical principles, regulatory guidelines and clinical pharmacology requirements in late stage clinical development.
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As lead of the Study Core Team the CS will lead via a matrix organization Epidemiology, Biostats, Clinical Operations, Medical/Scientific Affairs, Regional, Pfizer laboratory assay group, and external team members.
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Design, develop, validate, qualify, and implement clinical biomarker assays to support bioanalytical and clinical development of small molecule drug candidates. Experience with clinical assay development, validation, and qualification.
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clinical research affairs jobs Company: Biophase in San Francisco, CA
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