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Reporting directly to the Disease Team Project Manager, the Clinical Research Coordinator I is responsible for coordinating and managing clinical trials including providing all aspects of protocol management, including screening for patient eligibility, data collection and analysis, ensuring protocol compliance, 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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The Regulatory Coordinator I will act as a resource to investigators and staff for interpretation and execution of complex clinical research regulations, policies & procedures concerning the conduct of clinical trials, including those of the FDA, HHS, UCSD IRB, and the CTO. This position requires regular interaction with a variety of internal and external contacts including Cancer Center investigators and staff, UCSD IRB staff, study sponsors and/or their representatives.
$31.04 - $49.94 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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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.
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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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Meticulous and curious by nature, the Clinical Research Coordinator supports, facilitates, and coordinates the daily clinical trial activities and is instrumental in assuring the proper conduct of multiple trials.
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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 6 days ago - UpvoteDownvoteShare Job
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The Herbert Wertheim School of Public Health and Human Longevity Science (HWSPH ) and the Alzheimer’s Disease Cooperative Study (ADCS ) within the School of Medicine, Department of Neurosciences at UC San Diego have appointed a search for a joint-appointed associate or full professor rank faculty position in HWSPH Biostatistics and Neurosciences, with emphasis on clinical trials design, methodology, and conduct.
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The Clinical Research Coordinator is responsible for the overall coordination, organization, management, and efficient implementation of clinical trials. In executing these position responsibilities, the Clinical Research Coordinator is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.
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Experience reading and interpreting clinical trials research protocols. Advanced experience in Clinical Trials and Clinical Trials Program Management. Knowledge and experience of clinical research management and contract negotiation in an academic institution.
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Develop and maintain relationships with academic and community HCPs within assigned geography to provide on-label clinical and product education for BMS hematology products. 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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APP (DNP, NP), MSN, BSN with a minimum of 5 years clinical experience in a Hematology/Oncology Disease Area. As part of the commercial organization, the Clinical Nurse Consultant (CNC) is a trusted clinical expert responsible for developing professional relationships and educating key Health Care Professionals (HCP) involved in the care of patients receiving BMS hematology products in a defined geography.
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Targeting 10 years of experience as lead statistician on clinical trials in the pharmaceutical industry with significant experience in rare disease drug development. Responsible for overseeing the design, execution and interpretation of statistical analyses for clinical trials focused on rare disease.
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They will support/lead biomarker assay development and implementation, data analysis from clinical samples, and execute experiments to support translational strategies in early phase clinical trials across Fate’s iPSC derived NK and T cell platforms.
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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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Processes patient specimens for Fate's clinical trials to perform biomarker testing using multi-parameter flow cytometry and other cellular immunology assays. Fate Therapeutics is seeking a motivated individual skilled in immunology and/or cell biology to join our Clinical Translation team in support of the company's clinical trials utilizing off-the-shelf, iPSC derived immunotherapies.
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academic clinical trials jobs Company: Emory University in San Diego, CA
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