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Open nowPosted 17 days ago

Clinical Research Coordinator

MyCareersFuture94,028 open roles

Pay
SGD 3,550 – SGD 5,000 a month
Where
North, Singapore
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Your applicationOpen nowClinical Research CoordinatorMyCareersFuture · North, Singapore

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  2. 3.3%3 days
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  4. 14.0%14 days
  5. 33.7%30 days
This job: posted 17 days ago

The posting

  • Liaison person with Principle Investigator (PI), site-PI and various departments for clinical research procedures e.g. Specialist Clinics, Laboratory, wards, etc.
  • Plan, organise and coordinate the workflow of the research study
  • Adhere to protocol procedure
  • Screen research participants for eligibility according to research protocol
  • Enrol research participants and ensure their compliance to research procedures
  • Explain protocol to research participants and ensure that informed consent is taken as per
  • International Council of Harmonisation Clinical Practice (ICH-GCP) and Human Biomedical Research Act (HBRA) requirements
  • Schedule appointments for research participants within the time frame required in the protocol
  • Arrange for clinical/ laboratory tests and investigations; update schedule visit logs
  • Draw, centrifuge blood specimens and send specimens to laboratory or store specimens in accordance with requirement of research protocol
  • Assist in the completion and maintenance of biological specimen logs
  • Tracing and returning of case notes, blood results and all other results required in the protocol.
  • Assist with the completion and maintenance of investigational product receipt, storage, accountability, dispensing and disposal records
  • Assess subject’s condition; coordinate physical examinations per protocol; record medical drug history according to protocol
  • Collect and maintain data, as well as provide study reports
  • Documentation of patient reimbursement logs Filing and documentation of paper and electronic case report forms
  • Maintain investigator files and source documentation for each patient accordance to protocol requirements.
  • Identify, document and submit protocol deviations to Institutional Review Board (IRB) according to hospital and sponsor procedures
  • Inform PIs, Co-Investigators, collaborators and study team members on any adjustments based on protocol change
  • Complete, report and follow up on unanticipated problems involving risk to subjects and adverse events and/or serious adverse events
  • Traveling to research participants’ house may be required

Others

  • Perform quality checks on studies as Institution Monitor (where applicable)
  • NHG Committee of Practice (CoP) or Faculty member in CRC Society (where applicable)

JOB REQUIREMENTS

(A) EDUCATION, TRAINING AND EXPERIENCE

  • Degree in health sciences, nursing, pharmacy, clinical research or related field
  • Minimum Diploma or specialized diploma in the above
  • At least 3 years of experience in conducting clinical trials or research
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