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Nanyang Technological University

Project Officer - Clinical Research

Medical ResearchUpdated on Nov 14
Full-timeSingaporeNo salary listed

About the Job

Requirements

  • A bachelor's degree in Biological Sciences, Biomedical Sciences, Life Sciences, Psychology, Public Health, Nursing, or a closely related field is required.
  • Prior practical experience supporting clinical, health-related, or human-participant research is required, including participant coordination, questionnaire administration, data collection, or study documentation.
  • Willingness and ability to travel regularly to participating Traditional Chinese Medicine clinics and other research sites across Singapore is required.
  • Good spoken and written communication, clear interpersonal communication, and the ability to engage respectfully with participants and multidisciplinary healthcare teams are required.
  • Strong organisation, scheduling, record-keeping, and attention to detail are required, along with the ability to manage several study sites and meet research timelines.
  • Proficiency in Microsoft Office and electronic data entry is required.
  • The ability to safeguard confidential participant and sensitive mental-health data and appropriately report protocol deviations, adverse events, and safety concerns to authorised personnel is required.

Responsibilities

  • Support day-to-day implementation of the multi-site research programme across participating Traditional Chinese Medicine clinics, including regular on-site visits and coordination with site personnel.
  • Assist with participant identification, eligibility screening, informed consent, recruitment, enrolment, and allocation-related administrative procedures in accordance with approved research protocols.
  • Schedule research visits and follow-up assessments, maintain communication with participants, provide appointment reminders, and support participant retention throughout the study.
  • Administer validated questionnaires and clinical outcome assessments, ensuring accurate data collection, entry, verification, and management.
  • Coordinate biospecimen collection activities, including scheduling, labelling, tracking, and transportation arrangements, in collaboration with authorised clinical and laboratory personnel and in accordance with approved standard operating procedures.
  • Maintain accurate research documentation, including recruitment logs, participant records, study progress trackers, and protocol deviation reports, while promptly escalating adverse events and participant safety concerns to appropriate research or clinical personnel.
  • Collaborate with Principal Investigators, Traditional Chinese Medicine practitioners, and other research partners to support multi-site coordination, ethics submissions, regulatory compliance, research monitoring, and progress reporting.

Desired Qualifications

  • Prior data management experience is advantageous.
  • Familiarity with research ethics, informed consent, Good Clinical Practice, or clinical research standard operating procedures is desirable.

About the Company

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