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IRD Global Health, Research and Development, Singapore                 Job Code: HRD-PC/TD-406                                                                         Qualification:

  • Bachelor’s in Health Sciences or closely related field   


  • 1 to 2 years of relevant experience             

Jobs Responsibilities:

  • Responsible to monitor the quality of data captured and entered on documents of a phase III randomized controlled trial.
  • Responsible to ensure this is in accordance with the protocol, good documentation practice and Good Clinical Practice (GCP).
  • Responsible to maintain the Investigator Site File (ISF) and the Central Investigator File (CIF) for the Clinical Trial.

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