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You will assist investigators with the overall administration of clinical research activities before, during and after studies. This includes enrolling suitable subjects, taking vital signs, collecting and processing biological samples, entering data and monitoring subjects' condition. You will work with the study team to ensure subjects' safety and follow SOPs, study protocols and manuals in line with regulations and ICH Good Clinical Practice. You may also attend investigator meetings locally or overseas and liaise with internal and external agencies.
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