Job Role / Responsibilities:
You will be responsible to:
support the day-to-day clinical and research activities of the Clinical Trials Unit under the supervision of the principal investigator and CTU supervisorscoordinate and schedule study participants’ visits in accordance with approved research protocolsfacilitate patient care and perform clinical procedures including vital signs monitoring, IV cannulation, ECG, phlebotomy and specimen collectioncoordinate with pharmacists, oncology nurses and other relevant departments for study medication dispensing and administrationprocess, handle, store and dispatch biological specimens in compliance with laboratory and research protocolsmaintain accurate clinical, laboratory and research documentation, including source records, specimen logs, inventory records and temperature logsensure compliance with ICH-GCP guidelines, institutional policies, infection control mea...