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IQVIA Holdings Inc
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Charleston, WV
Assures clear client and internal team communication, process documentation, and compliance with Good Clinical Practices and procedures set forth by IQVIA Biotech and its clients....
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2 days ago
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Hospital Corporation of America
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Nashville, TN
Trial Manager you will plan the execution and monitor the completion of complex Phase I-IV assigned clinical research protocols....
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2 days ago
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23Andme, Inc
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San Francisco, CA
What youll do * Lead cross-functional study management teams responsible for the direction and oversight of Phase 1-3 clinical trials. * Lead the CRO and critical vendor selection process for outsourced...
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1 day ago
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University of Colorado
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Aurora, CO
works with Phase I-IV industry-sponsored, co-operative group and or investigator-initiated clinical trials in accordance with the trial protocols, FDA Regulations, and ICH/GCP Guidelines....
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2 days ago
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University of Chicago
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Chicago, IL
research and clinical trials....
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2 days ago
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University of Chicago
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Chicago, IL
research and clinical trials....
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2 days ago
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Thomas Jefferson University
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Abington, PA
for the Institutional Review Board (IRB) and other regulatory bodies as required by the protocol to ensure compliance in a timely fashion.Maintains accurate subject log, tracks expenses, submits appropriate...
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2 days ago
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HCA
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Denver, CO
in hematology/oncology and/or transplant At least one year of experience in a clinical research setting At least one year of experience managing blood cancer and/or BMT clinical trials is preferred...
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1 day ago
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Thomas Jefferson University
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Philadelphia, PA
trials to assist investigators in organizing, gathering and compiling clinical research data.Organizes and maintains documentation required for clinical trial(s).Informs Principal Investigator and/...
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1 day ago
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IQVIA
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Kansas City, KS
of current ICH GCP guidelines and applicable regulations. + Able to mentor CRAs and more junior Clinical Trial Managers. + Able to qualify for a major credit card. + Valid driver's license; ability...
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19 hours ago
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The CSI Companies
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Orlando, FL
Administration (FDA) regulations and International Conference on Harmonization/Good Clinical Practices (ICH/GCP) guidelines....
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6 hours ago
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NYU Grossman School of Medicine
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Mineola, NY
Performs all responsibilities in accordance with Standard Operating Procedures, CAP accreditation, established guidelines and work instructions, and appropriate industry and Good Clinical Practices...
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20 hours ago
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Stanford University
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Stanford, CA
Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices....
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16 hours ago
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Indian River Memorial Hospital
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Vero Beach, FL
Communicates to sponsors, Institutional Review Board (IRB) and CCIRH Clinical Research Review Committee (CRRC), Serious Adverse Events (SAEs), Progress Reports, Informed Consent Forms (ICFs), amendments...
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14 hours ago
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University of Chicago
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Chicago, IL
research and clinical trials....
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10 hours ago
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