Job Responsibilities
- coordinate clinical trials, including but not limited to logistics coordination, facilities management, trial subject recruitment, study procedures coordination, risk management, data collection, document management, and facilitation of monitoring/audits/inspections; and
- undertake any other duties as assigned.
Job Requirements
- associate degree or a higher diploma, preferably in life/biomedical science or health care discipline;
- interest and/or experience in clinical research definitely would be advantageous;
- good interpersonal and communications skills to foster a healthy and effective work environment;
- a good command of written and spoken English and Chinese (including Putonghua);
- good computer knowledge; and
- independent and able to multitask and collaborate in a team.