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You will assist the Principal Investigator(s) to implement and coordinate research projects. Research project activities included screening, recruitment, events reporting, data entry, biological specimens collection and processing, maintaining of sites files, and research participants’ follow up. You will conduct phone interviews or questionnaires with the research participants. You are required to adhere to Good Clinical Practice (GCP) guideline, protocol and regulatory compliance. You will also be supporting the department with general administration. The selected candidate will be offered employment on 1 to 2-year renewable contractual terms.
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