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Covance
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Irvine, CA
Job Overview: Senior Clinical Research Associate Rare Disease Experience Required Home-Based Why settle for one thing when you can have everything....
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2 days ago
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Ascent
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Irvine, CA
., FDA, DEKRA, PMDA) audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation Practices, client internal SOPs, and US and OUS regulations (15%)...
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3 days ago
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Covance
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Irvine, CA
Experience: A minimum of at least 9 months of Onsite Clinical Monitoring experience and 2 years total in clinical research experience is required....
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6 days ago
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Cerritos, CA (20 miles from Irvine, CA)
Clinical Practice (GCP), Good Documentation Practice (GDP), Standard Operating Procedures (SOP), and department specific Work Instructions (WI).brPerform and complete study procedures, including but...
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12 days ago
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Covance
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Irvine, CA
Experience: A minimum of at least 9 months of Onsite Clinical Monitoring experience and 2 years total in clinical research experience is required....
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13 days ago
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Covance
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Irvine, CA
Experience: A minimum of at least 9 months of Onsite Clinical Monitoring experience and 2 years total in clinical research experience is required....
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16 days ago
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Integrium Llc
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Tustin, CA (4 miles from Irvine, CA)
Perform and coordinate all aspects of the clinical monitoring process in compliance with ICH/GCP guidelines and other regulatory agency guidelines....
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17 days ago
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Irvine, CA
timelines and study milestones + Oversight/execution of feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable...
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24 days ago
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Wcct Global
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Cypress, CA (17 miles from Irvine, CA)
Essential Job Functions Follow all study and non-study regulations including, but not limited to: Patient/Subject Privacy (HIPAA), OSHA, Good Clinical Practice (GCP), Good Documentation Practice(GDP...
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24 days ago
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Edwards Lifesciences Corp
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Irvine, CA
Trial Management System), eTMF (electronic Trial Master file) preferred Excellent written and verbal communication skills and interpersonal relationship skills Excellent problem-solving and critical...
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26 days ago
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Kelly Services
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Irvine, CA
timelines and study milestones + Oversight/execution of feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable...
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27 days ago
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Edwards Lifesciences
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Irvine, CA
The In house Clinical Research Associate II will ensure clinical trials are conducted and reported in accordance with all applicable regulatory requirements....
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27 days ago
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Syneos Health
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Orange, CA (6 miles from Irvine, CA)
The Senior Clinical Research Associate I (SCRA I)will perform monitoring and site management activities for Phase I-IV clinicalresearch projects to assess the progress of clinical projects at assignedinvestigative...
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29 days ago
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Johnson & Johnson
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Santa Ana, CA (6 miles from Irvine, CA)
Coordinate Institutional Review Board/ Ethics Committee (IRB/EC) approvals. Train site personnel to ensure compliance with study requirements....
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45+ days ago
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Sonendo, Inc
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Laguna Hills, CA (9 miles from Irvine, CA)
Clinical Practices, ICH Guidelines, CFR Guidelines, clinical research ethics, HIPAA and patient privacy laws (plus applicable local regulations, when country-based) Knowledge of concepts of clinical...
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45+ days ago
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Everything we do in healthcare has to be discovered and thoroughly tested before it can be put into practice. In this course you will explore clinical research – its...
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