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IRD Global Health, Research and Development and Development, Singapore          Position Code: HRD-PC/TD-398                    


  • Bachelor’s with a majors in Social or Health Sciences, Business Studies, Economics or a related field.
  • Certification in Good Clinical Practice, or Project Management. Microsoft Office (Excel, PowerPoint, Word etc.)
  • Undergo training about the protocol, trial procedures, good documentation practices and Good Clinical practices.

Jobs Responsibilities:

  • Manage operational and administrative requirements of the clinical trials, that are of significance to its existing and upcoming new sites for the day-to-day functioning of the clinic, field, pharmacy, lab, data, and quality assurance departments.
  • Represent the clinical trials to stakeholders including but not limited to sponsors, implementing partners, collaborators, regulatory and ethical bodies.
  • Analyze, design, document, and implement internal reporting systems and policies for the clinical trial sites within specified areas of operations (e.g. patient/clinic flow, procurement planning and execution, orientation/on-boarding for new joiners, etc), with the aim of supporting the efficient implementation of trial protocols, Manual of Procedures (MOPs) and SOPs within the project’s budgeted resources.

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