- Liaison person with Principle Investigator (PI) and site-PI.
- Liaison person with various departments for clinical research procedures e.g. Specialist Clinics, Laboratory, wards, etc.
- Adherence to protocol procedure.
- Screening and recruiting suitable candidates as research participants.
- Explain protocol to research participants.
- Ensure that informed consent is taken as per Singapore Good Clinical Practice (SGGCP) requirements.
- Contact and schedule appointments for research subjects within the time frame required in the protocol.
- Centrifuge blood specimens and send specimens to laboratory.
- Tracing and returning of case notes, blood results and all other results required in the protocol.
- Responsible for data collection and performing research procedures.
- Documentation of patient reimbursement logs
- Filing and documentation of paper and electronic case report forms.
- Maintain source documentation for each patient accordance to protocol requirements.
- Identify, document and submit protocol deviations to Domain Specific Review Board (DSRB) according to hospital and sponsor procedures.
- Inform PIs and collaborators on any adjustments based on protocol change.
- Identify and document Adverse Events (AE), if any, and obtain the PI’s signature.
- Work with in-house Research Database IT Specialist on extraction of patient medical records and data mining.
- Traveling to research participants’ house may be required.
GENERAL (10%)
- To participate in projects and activities as assigned by Director, Clinical Research Unit
EDUCATION, TRAINING AND EXPERIENCE
- Minimum Diploma in Biomedical Science or equivalent
- Experience as Clinical Research Coordinator preferred
