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Clinical Research Associate

Natural wellness
Nasr City, Cairo
Posted 5 years ago
143Applicants for1 open position
  • 98Viewed
  • 13In Consideration
  • 75Not Selected
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Job Details

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Job Description

  • Ensure the delivery of Phase II or Phase III clinical trial within the time frame, and are conducted in accordance with G.C.P and applicable ethical and regulatory requirements, SOPs and project Gantt chart.
  • Act as the mainline of communication with the principal investigators and his/her team and the CRO.
  • Follow up the procedures for manufacturing, dispensing, and return of investigational product(s) and ensure that they are safe, adequate and properly documented in accordance with local regulations and the trial protocol.

Job Requirements

  • Knowledge of GCP principles, Clinical studies procedures and guidelines.

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