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IQVIA Holdings Inc
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Los Angeles, CA
Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research....
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9 hours ago
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Three Point Solutions
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Los Angeles, CA
International clinical trial management experience....
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1 day ago
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PPD
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Los Angeles, CA
Clinical Trial Management System). Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts....
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4 days ago
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Cedars-Sinai
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Los Angeles, CA
The Clinical Research Specialist I - Investigator Initiated Trials will develop processes for investigator initiated trials including: developing process workflows, manuals, standard protocol language...
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6 days ago
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Cedars-Sinai
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Los Angeles, CA
Review Board....
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7 days ago
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PRA Health Sciences
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Los Angeles, CA
), ICH-GCP, and all applicable regulatory requirements....
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11 days ago
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PRA Health Sciences
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Los Angeles, CA
As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported...
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11 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 the Principal Investigator or directly with the Institutional Review Board to submit Adverse Events...
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14 days ago
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AbbVie, Inc
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Los Angeles, CA
Ensure adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality...
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15 days ago
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City of Hope (Duarte, CA)
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Duarte, CA (19 miles from Los Angeles, CA)
Assists in training and mentoring new clinical research staff members. Performs protocol specific clinical duties as required per the research study....
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30+ days ago
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Cedars-Sinai Medical Center
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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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30+ days ago
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Cedars-Sinai Medical Center
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Los Angeles, CA
As a Clinical Research Associate II, you will also be responsible for the following: Ensure compliance with protocol and overall clinical research objectives, while maintaining research practices using...
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30+ days ago
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Cedars-Sinai
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Los Angeles, CA
Click here Job Seeker Find A Job Browse Jobs New Job Listings Veterans Quick Subscribe Create an account Schedule A Demo Clinical Research Associate II - Oncology Clinical Trials Job Listing at Cedars-Sinai...
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30+ 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 the Principal Investigator or directly with the Institutional Review Board to submit Adverse Events...
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30+ 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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30+ days ago
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