Position: Research Assistant
Responsibilities:
- Serve as the liaison between the Principal Investigator (PI), site-PI, and various departments involved in clinical research, such as Specialist Clinics, Laboratory, and wards.
- Ensure adherence to protocol procedures.
- Screen and recruit suitable candidates as research participants.
- Explain the protocol to research participants and obtain informed consent in accordance with ICH GCP guidelines and the Human Biomedical Research Act (HBRA).
- Schedule appointments and contact research subjects within protocol-specified timeframes.
- Centrifuge blood specimens and send them to the laboratory.
- Trace and return case notes, blood results, and other relevant data as required.
- Collect data and perform research procedures accurately.
- Maintain documentation of patient reimbursements, case report forms (both hardcopy and electronic), and source documentation according to protocol requirements.
- Identify, document, and report protocol deviations to the Institutional Review Board (IRB) following hospital and sponsor procedures.
- Notify PIs and collaborators of any protocol adjustments.
- Report and follow up on unanticipated problems, risks to subjects, adverse events, and serious adverse events.
- Collaborate with the Research Database IT Specialist for data extraction and mining from medical records.
- Travel to participants' homes may be required.
Additional Activities:
Participate in projects and activities assigned by the Director of the Clinical Research Unit.
Job Requirements:
(A) Education, Training, and Experience
- Minimum Diploma in Biomedical Science or equivalent.
- Experience as a Research Assistant is preferred.