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Identify, engage, and manage the activities of clinical CROs and other clinical study providers (e.g., core labs, Electronic Data Capture (EDC) providers, and independent contractors) to execute clinical trials.
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The Research Coordinator will assist in the conduct of Clinical Trials by ensuring protocol compliance, filing adverse drug reaction reports, monitoring patient treatment and toxicities, laboratory and specimen submission, and maintenance of accurate and complete clinical research files.
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Near-term focus will be on leading the legal support for supply chain, clinical trials and regulatory issues and will evolve to also include supporting commercialization capabilities. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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The Clinical Trials Office (CTO) at UCSD's Moores Cancer Center administers many clinical trials on behalf of its member investigators, including trials sponsored by National Cancer Institute cooperative groups, pharmaceutical companies, and physician investigators.
$71,000 - $160,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience in optimizing and delivering peptide-protein conjugates as candidates for clinical trial. Lead projects and teams towards agreed upon goals, ultimately working towards clinical candidate peptide nomination.
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Scientific and Operational Leadership : Lead biomarker data collection in clinical trials and non-interventional studies, ensuring robust and reliable data. This position offers the opportunity to build and lead a world-class biomarker team in a fast-growing company, ensuring the seamless integration of biomarker assays into clinical trials and robust clinical data management.
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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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MINIMUM QUALIFICATIONSQualified candidates must possess:Licensure by the State of California as a Psychologist; AND,Graduation from an accredited U.S. college or university, or certified foreign studies equivalency with a Ph. D. or Psy. D. in clinical, community or educational psychology; AND,Four (4) years post-doctoral experience in a mental health, forensic or correctional setting.
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The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
$23.39 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California, is an academic institute comprised of an expert panel of scientific collaborators, committed to advancing the development of new treatments for Alzheimer’s Disease (AD) through innovative clinical trials.
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Certifications/Licenses MLS/MT(ASCP)CM or equivalent experience CA Clinical Laboratory Scientist (CLS) required CA Clinical Immunohematologist Scientist (CIS) preferred Specialist in Blood Banking (SBB) certification preferred Experience : Up to three (3) years of Laboratory experience.
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QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine.
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Provide operational leadership for one or more of Avidity’s programs, including demand/supply/capacity planning, sourcing, clinical labeling, packaging, inventory management, cold chain shipping, import/export, and distribution.
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The Medical Science Liaison (MSL) is considered the field- based scientific and clinical expert on current and future Innovative Medicine Oncology products. Compliantly collaborate with internal stakeholders including but not limited to MSL field partners, R&D, US as well as Global Medical Affairs teams, clinical operations, sales, and marketing teams.
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Minimum 4 years of experience in a clinical laboratory as a Clinical Lab Scientist or Medical Technologist required. Bachelors degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements.
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clinical trials jobs Title: nurse practitioner in San Diego, Wells, Nevada
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