Assist the investigators in overall administration of clinical research activities prior to, during, and post-study, such as enrolling suitable subjects, taking vital signs, collecting and processing biological samples, collecting and entering data, and monitoring 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 meetings (local/overseas) and site initiation meetings as assigned and liaise with relevant internal and external agencies during the course of work.
Requirements:
Degree in Sciences/Nursing. Those with a Diploma will be considered as Associate.
Registration with the Nursing Board, Singapore (applicable to State Registered Nurse only).
At least 2 years of experience in the coordination of clinical research activities.