Responsibilities:

Assist the investigators in overall administration of clinical research activities prior to, during and post study such as enrol suitable subjects, take vital signs, collect and process biological samples, collect and enter data, monitor subjects’ condition

Work with the study team to ensure subjects’ safety

Carry out the required procedures according to the SOP, study protocol and Instruction manual(s) and in compliance with the Regulations and ICH Good Clinical Practice Guideline

Attend investigator’s meeting (local/overseas) and site initiation meeting as assigned and liaise with relevant internal and external agencies during the course of work

Any other duties assigned from time to time

Requirements:

Bachelor’s degree in Sciences, Nursing, Biomedical or any other discipline.  Those with Diploma will be considered as Associate Clinical Research Coordinators

2 years of working experience in coordination of clinical research activities

Strong interest and passion in research

Good interpersonal & communication skills

Only shortlisted candidates will be notified