Press Tab to Move to Skip to Content Link
Select how often (in days) to receive an alert: Create Alert
Job Responsibilities:
- Liaison person with Principal Investigator (PI) and site-PI.
- Liaison with various departments for clinical research procedures, e.g., Specialist Clinics, Laboratory, wards, etc.
- Adherence to protocol procedures.
- Screening and recruiting suitable candidates as research participants.
- Explain protocol to research participants and ensure informed consent is obtained in accordance with ICH GCP and HBRA requirements.
- Schedule appointments for research subjects within the required time frame.
- Centrifuge blood specimens and send to laboratory.
- Trace and return case notes, blood results, and other protocol-required results.
- Responsible for data collection and performing research procedures.
- Maintain documentation of patient reimbursement logs, and case report forms (hardcopy and electronic).
- Maintain source documentation for each patient as per protocol.
- Identify, document, and submit protocol deviations to IRB following hospital and sponsor procedures.
- Inform PIs and collaborators of any protocol changes.
- Report and follow up on unanticipated problems, adverse events, and serious adverse events.
- Collaborate with in-house Research Database IT Specialist on data extraction and mining.
- Travel to participants’ homes may be required.
Job Requirements:
(A) Education, Training, and Experience
- Minimum Diploma in Biomedical Science or equivalent.
- Experience as a Research Assistant preferred.