Clinical Research Associate @ Harich Corporate

Job Description

• Identifying/selecting an investigator who will be responsible for the conduct of the trial at the trial site.
  
• Liaising with doctors/consultants or investigators on conducting the trial.
• Verify that investigator and investigators team are adequately trained and comply with the protocol.
• Verify that IRB/IEC operates and complies as per GCP, SOP and applicable regulatory requirements.
• Monitoring the trial throughout specified duration involving monitoring visit to the trial sites.
  
• Source data verification
• Writing visit reports, filing and collecting trial documentation and reports.

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