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Research Assistant, Department of Medicine

Salary undisclosed

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Job Overview

To assist investigators in conducting clinical trials and research according to study protocol, ICH Good Clinical Practice (ICH GCP), Singapore Human Biomedical Research Act (HBRA) and other applicable regulatory and ethical requirements as well as hospital policies.

Primary Responsibilities and Duties (90%)

  • Compliance with the ICH GCP, HBRA and other applicable regulatory and ethical requirements as well as hospital policies if applicable
  • Assist in communications with DSRB/IRB staff regarding study-related ethics applications, amendments and status reports.
  • Attend trial-related initiation, close-up and other trial related meetings
  • Complete Case Report Forms (CRFs)
  • Handle data entry and validation of study data
  • Label and dispatch specimens to the relevant laboratory as in the condition as specified in the trial protocol
  • Label and store specimens in the condition as specified in the trial protocol
  • Maintain Investigator Site File and ensure that all study documents are complete and up-to-date
  • Trace laboratory and diagnostic reports (if any)
  • Assist the investigator(s) in adverse events / serious adverse events reporting
  • Maintain confidentiality on trial data
  • Assist Investigators in the screening, recruitment, assessment and follow-up visits of potential patients/healthy volunteers
  • Assist Investigators in obtaining informed consent
  • Schedule appointments for patients/subjects
  • Procurement of consumables and subject reimbursement
  • Liaise with relevant internal and external agencies during the course of work
  • Perform administrative duties and ad-hoc projects as assigned by the supervisor.
  • Record, analyse and present findings of research activity for review purposes
  • Help prepare progress reports on research