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Clinical Research Coordinator (Contract)

On-site Singapore contractor

Job Description

You will assist Principal investigators in conducting clinical trials & research projects according to Singapore Good Clinical Practice (GCP) guidelines. You will plan, organise & coordinate workflow of study projects from initiation to completion phase, perform screening and recruitment activities as well as compile relevant patients' data and maintain proper study documentation according to established protocols and regulatory requirements. Additionally, you will facilitate coordination of research studies with funding and regulatory bodies. Other duties include providing administrative support for Research Department when the need arises.

Requirements:

  • Life Science or Nursing Degree holder. Candidates with Nursing Diploma must have minimum 2 years of relevant experience
  • At least 1-2 years of experience in clinical research coordination
  • Ability to converse in mainstream languages (able to speak in local dialects will be an added advantage) to handle patient queries on the research study
  • Strong organizational skills, able to work independently and/or a team player, meticulous in details
  • Proficient with MS Office applications

Source: the employer's careers page. Last checked 2026-10-18. Posted 2026-10-10.

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