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Assist with Otsuka's clinical trials program, including registrational, post-marketing and Investigator-Sponsored Trials (ISTs), health economic outcomes research, other specific medical collaborations; provide clinical expertise and feedback regarding operational management of clinical trials to ensure optimal site selection and performance.
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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
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As such, you will provide scientific input into design & implementation of clinical trials, their delivery, clinical data review and data cleaning, interpretation of results, reporting successfully on time, and activities required for worldwide registration of the product ( clinical input to NDA/BLA.
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It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials, local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as clinical database and biorepository.
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Collaborate with translational research teams to develop and implement sample management system for appropriate handling, storage, and documentation of preclinical and clinical samples. A dynamic research environment dedicated to the pursuit of clinical discovery research by leveraging high-content multimodal clinical and biomarker data to develop the next generation of therapeutic targeting strategies.
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Prior experience in providing MSL-level support to products or devices in endocrinology and/or rare disease, including KOL development, investigator-initiated clinical trials, publications and educational programs, highly preferred.
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Design, implement and monitor FACS derived biomarker and diagnostic testing as well as data collection in early pre-clinical and clinical trials. In turn, these high-quality cell-based biomarker approaches rapidly inform on biomarker strategy in the preclinical and early clinical trial setting and directly impact phase I clinical dosing decisions.
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The Division of HIV, Infectious Diseases and Global Medicine at the University of California San Francisco (UCSF) is an internationally recognized global leader in clinical care, research, and education.
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The Department of Translational Medicine leads biomarker discovery and development efforts for programs in Early Stage Research through Phase III clinical trials for the disease areas of Ophthalmology, Metabolism, Neuroscience, Immunology and Infectious Diseases (TM-OMNI.
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Oversee daily operations of clinical services for Community Forward within these programs: A Woman’s Place, A Woman’s Place Drop-In Center, Permanent Supportive Housing sites, and ReEntry programming.
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Experience with therapeutic programs that have yielded drugs entering clinical development in endocrinology, diabetes/obesity, immunology/inflammation, or metabolic disease. Proficiency with cell-based assays, ELISA, MSD, qPCR, RNseq, microscopy, histology/pathology (e.g., IF/IHC/ISH), and/or flow cytometry.
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The Clinical Quality Measurement team manages HEDIS annual submissions and other quality measure submissions to CMS, NCQA, DHCS and other governing bodies. Recommend and implement solutions for identified problems/root cause pertaining to clinical data used for HEDIS reporting.
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License Required: California Clinical Laboratory Scientist or Clinical Genetic Molecular Biologist Scientist (for Applied Genomics and Hemoglobinopathy Labs Only) license required. Position Summary: The clinical laboratory scientist performs routine and complex laboratory procedures in a prompt, accurate and reliable manner according to established policies, procedures and quality control guidelines.
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Marriage and Family Therapist, Licensed Professional Clinical Counselor, or Clinical Psychologist preferred. The CSP Clinic Director is responsible for the overall leadership, management, and operation of the clinical training program, working collaboratively with CIIS Administration, and supervising the Clinic Manager.
$68,000 - $76,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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CERTIFICATION & LICENSURE: Certified Clinical Documentation Specialist (CCDS) or Certified Documentation Improvement Practitioner (CDIP)Certified Coding Specialist (CCS) or Certified Professional Coder (CPC)SKILLS AND KNOWLEDGE:Knowledge of Pathophysiology and Disease Processes sufficient to pass the clinical pre-employment test at a rate of 85% or better is required for new hires.
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clinical trials jobs Title: coordinator Company: University Of California in San Francisco, CA
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