Clinical Research Coordinator

2 weeks ago


Singapore National Skin Centre(S) Pte Ltd Full time

  • Family Group: Allied Health

Statement of Purpose
To facilitate clinical research activities in the hospital

MAJOR DUTIES AND RESPONSIBILITIES

  • Liaison person with Principle Investigator (PI), sitePI 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
  • 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
  • Traveling to research participants' house may be required

Leadership
Mentor junior clinical research staff

Others

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

General

  • To participate in projects and activities as assigned by Director, Clinical Research Unit

EDUCATION, TRAINING AND EXPERIENCE

  • Degree in health sciences, nursing, pharmacy, clinical research or related field
  • Minimum Diploma or specialized diploma in the above fields


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