Clinical Research Assistant in Santa Clara, CA

Candidates should have some Clinical Trial Experience so they understand documents and are familiar with terminology.

• Responsible for assisting the Clinical Research Associate in conducting Phase I - IV clinical studies according to ICH guidelines.
• The major role is to begin learning CRA work including verifying the content of critical regulatory documents, writing basic protocols, monitoring clinical sites, and reviewing case report forms (CRF's).
• 0-3 Years Experience Level.

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