Menlo Park, CA
Review Board (IRB) submission and compliance management Align operational aspects of research with the needs of other internal stakeholders including engineering, legal, and product requirements Assist...
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11 hours ago
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PAREXEL
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Needles, CA
Your time here At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor....
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1 day ago
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PAREXEL
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Needles, CA
Your time here At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor....
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2 days ago
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Pharmaceutical Research Associates
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San Diego, CA
Clinical Research Associate 1 - PHARMA - SoCA/AZ/NV US-CAUS-AZUS-NV Job ID: 2021-73981 Type: US-Southeast # of Openings: 1 Category: Clinical Monitoring GSK Overview Do you want to watch clinical development...
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1 day ago
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Glaukos Corporation
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San Clemente, CA
Regional Principal Clinical Research Associate San Clemente, CA Share Posted 1 day ago Apply Now Processing... Email Job Apply Now Processing......
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16 hours ago
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Cedars-Sinai
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Los Angeles, CA
Assists with regulatory submissions to the Institutional Review Board (IRB) and works closely with supervising research staff or directly with the Institutional Review Board to submit Adverse Events...
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16 hours ago
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Pharmaceutical Research Associates
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San Diego, CA
Responsibilities What you will be doing: The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted...
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1 day ago
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Scripps Health
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San Diego, CA
Coordinates multiple aspects of clinical trials and other human research ensuring compliance with research protocol and IRB requirements....
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4 days ago
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PRA Health Sciences
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Santa Monica, CA
You want to push the boundaries and change not just what it means to be a Clinical Research Associate, you want to change the future....
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4 days ago
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PRA Health Sciences
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Santa Monica, CA
You want to push the boundaries and change not just what it means to be a Clinical Research Associate, you want to change the future....
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4 days ago
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Cedars-Sinai
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Los Angeles, CA
Assists with regulatory submissions to the Institutional Review Board (IRB) and works closely with supervising research staff or directly with the Institutional Review Board to submit Adverse Events...
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4 days ago
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Guardant Health
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Redwood City, CA
Job Description The Clinical Research Associate II (CRA II) is responsible for management and monitoring activities that will lead to successful execution of clinical studies....
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4 days ago
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Guardant Health
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Redwood City, CA
Job Description The Senior Clinical Research Associate is responsible for management and monitoring activities that will lead to successful execution of clinical studies....
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4 days ago
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Progenity, Inc.
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San Diego, CA
The Clinical Research Associate I (CRA I) is responsible for the day-to-day operational oversight of clinical trial sites in the United States (or worldwide, as necessary)....
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6 days ago
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Cedars-Sinai
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Los Angeles, CA
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
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6 days ago
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