Clinical Research Associate - Sydney
3 weeks ago

Job summary
+Overseeing clinical trials/studies involved in each step of the clinical study.+Preparing protocols required for trial approval by EC.<+Monitoring and coordinating the clinical trial conduction following GCP and SOP strictly.+Ensuring all SAEs/adverse drug reactions are reported in a timely manner according to internal relevant SOP.+-Qualifications
- Bachelor degree in biomedical/science discipline. -
- At least 3-6years clinical operation monitor experience. -
- Fluent English -
Job description
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