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The Department of Medicine at the University of California San Francisco (UCSF) is recruiting for a Clinical Investigator (MD/DO or PhD/DrPH/ScD trained) to join the faculty as an Assistant, Associate, or Full Professor in the Division of General Internal Medicine (DGIM) at Zuckerberg San Francisco General Hospital and Trauma Center (SFGH.
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Verifies information with clinical research nurse and/or principal investigator. We are currently recruiting a Clinical Research Coordinator to work alongside Drs. Mouhsin Shafi and Stephanie Buss on studies involving Transcranial Magnetic Stimulation (TMS) and Alzheimer's disease.
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The investigator-initiated clinical trial management supervisor will work very closely with USC/Norris Cancer Center physician-scientists, various CISO services and teams, Data Science Shared Resource and other cancer center core services to ensure that IITs are of the highest quality.
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For CRA I: 1+ years direct clinical research experience at a sponsor, CRO, device manufacturer, IVD, companion diagnostics or investigator site. Maintain the study Trial Master File (TMF)/or eTMF and ensure the Investigator Site Files (ISFs) are current and maintained.
ExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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The Clinical Research Coordinator II works within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DF/HCC Clinical Trials Office and/or Partners HealthCare Institutional Review Board (IRB.
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This initiative is comprised of the Robert A. Winn Career Development Award (Winn CDA) for early-stage investigator physicians who are underrepresented in medicine or who have a demonstrated commitment to increasing diversity in clinical research, and the Robert A. Winn Clinical Investigator Pathway Program (Winn CIPP) for medical students underrepresented in medicine.
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The Clinical Research Coordinator assists the investigator team to develop study protocols and manuals of procedures. The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials in cardiovascular and chronic kidney diseases.
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The Clinical Research Coordinator assists the Primary Investigator in all IRB and regulatory submissions and clinical coordination specific to protocol. The incumbent functions independently under minimal supervision, following COG , FDA , Good Clinical Practice, IRB , NIH , NCI , NSF and/or other regulatory agency guidelines and seeking council from the Principal Investigator as necessary.
$39,300 - $64,349 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The clinical research coordinator will work closely with the principal investigator, Dr. Desmond Oathes. The clinical research coordinator (CRC) will be trained to conduct human neuroimaging research with a number of tools, including administration of TMS inside and outside of an MRI scanner.
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Develop and serve as principal investigator for investigator-initiated clinical trials in radiation/oncology. Clinical research is conducted through the excellent Cancer Center translational research infrastructure that includes the minority based NCORP grant, Cooperative group trials, investigator-initiated trials and the Phase I and II clinical research programs.
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The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI) and Sub-Investigator (SI.
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The individual will be responsible for assisting the Pediatrics Department Chair and other faculty in conducting National Institute of Health (NIH), industry sponsored clinical trials, and/or investigator-initiated trials.
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The Staff Scientist I is a junior career research position that reports to the principal investigator. Conducts research and development of new next generation sequencing clinical assays.
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The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator and Scientific Director.
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Reporting to the Lead Clinical Research Associate, the CRA II/Sr. CRA will perform quality and compliant Investigator site monitoring and relationship-driven Investigator site management in line with MapLight’s SOPs, our Mission, Vision, and Values, as well as industry quality and regulatory best practices (ICH GCP.
ExpandApply NowActive JobUpdated 16 days ago
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