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We deviate from traditional models of drug development by focusing on performing science that gives our drugs the best chance to succeed in clinical trials. Based in downtown San Diego, California, Novoron Bioscience is a startup biotechnology company pioneering lipoprotein-receptor drug development to repair damage and degeneration to the brain, spinal cord and beyond.
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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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As the cornerstone of clinical research, the Clinical Research Coordinator is responsible for facilitating protocol related guidance regarding compliance, personnel and other relevant aspects of trials at multiple research sites, medical institutions, CRO's and Sponsors.
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Our Motility Center has participated in several multicenter trials and collaborations with UCSD bioengineering. As a member of the Health Sciences Compensation Plan, the appointee should be aware that there are limitations on outside professional activities, and clinical moonlighting is expressly prohibited.
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Its medical services include advanced surgery, cancer care, cardiac rehabilitation, clinical trials, birthing options and more. According to US News and World Report Survey, UCSD health is ranked number one in San Diego, placing it among the nation's best hospitals.
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The Lead Clinical Research Coordinator will plan, develop and implement start-up procedures for multiple phase I-IV research studies in Interventional Cardiology Clinical Trials as well as lead, direct, and coordinator operational efforts.
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Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.
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In-depth knowledge of Oncology and Immunology clinical trials, including protocol design, patient recruitment, and monitoring, with a demonstrated ability to navigate the unique challenges associated with neurological disorders.
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Other duties as assigned by the Program Coordinator or the Associate Dean/Founding Program Director. UCSD Layoff from Career Appointment : Apply by 03/21/2024 for consideration with preference for rehire.
$19.49 - $39.2 an hourFull-timeExpandUpdated Yesterday - UpvoteDownvoteShare Job
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Ensure conduct of clinical trials in compliance with GCP/ICH regulations and guidelines, and applicable SOPs and Work Instructions. Experience in early phase oncology (preferably solid tumor) clinical trials is required.
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The CRC will participate in and manage all administrative aspects of clinical trials communicating with Doctors, Nurses, and Sponsors daily. Schedules and organizes monitor and sponsor on-site visits, as needed, including setting up pharmacy, lab, and Principal Investigator (PI) meetings with the Clinical Research Associate.
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Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and company SOPs. Execute assigned clinical trials including start up, subject recruitment & scheduling, consenting, screening, subject training, collection of regulatory documents, conducting study visits, performing SMBG testing, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, and providing IRB close-out reports.
$42 - $48 an hourExpandUpdated Yesterday - UpvoteDownvoteShare Job
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Our goal is to engage every healthcare professional in clinical research and to make clinical trials a care option for every patient. This role will perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.
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This role offers a flexible work-from-home arrangement, enabling you to engage in various activities such as online surveys, focus groups, clinical trials, product tests, and optional delivery services for food and groceries.
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How you will contribute to LifeNet Health’s success: The Clinical Research Associate is responsible for managing assigned clinical research trials and ensuring the trials are on schedule and in compliance with all regulatory requirements.
$111,170 - $185,284 a yearExpandApply NowActive JobUpdated 15 days ago
clinical trials jobs in La Jolla, CA
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