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Temporary Rehab Research Assistant (Until February 2026)

Posted on Nov. 6, 2025 by National Healthcare Group

  • temporary

Temporary Rehab Research Assistant (Until February 2026)
Institution: Khoo Teck Puat Hospital
Family Group: Allied Health

MAJOR DUTIES AND RESPONSIBILITIES

(A) SPECIFIC

  • Liaise with Principal Investigator (PI) and Project Manager on study-related matters.
  • Coordinate with various departments for clinical research procedures.
  • Ensure strict adherence to study protocol procedures.
  • Screen and recruit suitable candidates as research participants.
  • Explain study protocol to participants and obtain informed consent in accordance with ICH-GCP and HBRA requirements.
  • Schedule appointments for research subjects within protocol-defined timelines.
  • Conduct research procedures and collect study data accurately.
  • Maintain documentation of participant logs, including hardcopy and electronic data.
  • Maintain source documentation for each participant in accordance with protocol requirements.
  • Identify, document, and submit protocol deviations to the Institutional Review Board (IRB) as per hospital and sponsor procedures.
  • Inform PIs and collaborators of any adjustments due to protocol changes.
  • Complete, report, and follow up on unanticipated problems involving risk to subjects, including adverse and serious adverse events.
  • Collaborate with in-house Research Database IT Specialist for data extraction and mining.
  • Participate in projects and activities as assigned by the Director, Clinical Research Unit.

(B) GENERAL

  • Participate in process improvement initiatives and contribute to streamlining research workflows.
  • Work collaboratively with other departments and service providers.
  • Adhere to hospital and department standards in all duties.
  • Support corporate and departmental events when required.
  • Undertake other duties as assigned.

JOB REQUIREMENTS

(A) EDUCATION, TRAINING AND EXPERIENCE

  • Diploma or Degree in Life Sciences, Biomedical Sciences or related field.
  • Prior experience in clinical or biomedical research is advantageous.
  • Good communication and interpersonal skills.
  • Proficient in Microsoft Office and electronic data systems.
  • Familiarity with ICH-GCP and HBRA guidelines.
  • Able to work independently and within a multidisciplinary team.
  • Willing to work flexible hours depending on study requirements.


Advertised until:
Dec. 6, 2025


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