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Clinical Research, Associate I

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Abbott
πŸ“ Alameda, United States
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Location Alameda
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Posted June 12, 2026
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Commute Local Area
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Job Description

The Opportunity

The CRA will ensure quality, accuracy and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations, ICH GCP, and ISO14155.

This is an on-site position in Alameda, California.

What You’ll Work On

  • Perform internal clinical studies, recruit study participants, conduct informed consent discussions with study volunteers, record study data, and maintain study files.
  • Coordinate internal clinical studies from start to close-out.
  • Perform study site visits (SQV, SIV, IMV, COV), generate monitoring reports, and track resolution of action items.
  • Assist and conduct clinical monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures, and other applicable regulatory requirements.
  • Participate in study start up ...
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    πŸ“ Location Details

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    City
    Alameda
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    Country
    United States
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    Commute
    Local Area

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