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Senior Clinical Research Associate

📍 Agilent • Beijing, Beijing, China • Posted June 21, 2026

Full time Posted June 21, 2026
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Job Description

Description

  • Responsible for scheduling and conduct of pre-study visits, initiation visits, interim monitoring visits and close-out visits according to the Monitoring Plan.
  • Ensures the HGRAC and IRB submission and approval.
  • Ensures assigned sites are conducting studies according to protocol requirements and applicable regulations and guidelines.
  • Ensure that the rights and wellbeing of human subjects are protected.
  • Ensure the trial data are accurate, complete, and verifiable from source documents.
  • Verifies that the investigator is enrolling only eligible subjects.
  • Performs verification of source documents against Case Report Form/Electronic Data Capture entries to assure accurate and complete data.
  • Ensures that any corrections are appropriately documented by authorized site staff.
  • Performs Investigational Product accountability, including product storage, inventory, return/destruction, and dispensi...

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