AbbVie Medical Science Liaison in Guangzhou (Canton), China
Overseeing the management and administration of all aspects of clinical trials/studies involved in each step of the clinical trial/study. Assisting with preparation of protocols and other necessary documents required for trial approval by HA. Preparing protocols and other necessary documents required for trial approval by EC and getting EC approval on time. Monitoring and coordinating the clinical trial conduction in whole process by following GCP and SOP strictly. Coordinating and giving input to all activities including query resolution, site closure and collection of documentation required for clinical trial reports after trail end. Ensuring but not limited to, IMPACT, EDC system for administration of clinical trials is updated in a timely and accurate manner in accordance with requirements. Ensuring all SAEs/adverse drug reactions are reported and followed up in a timely manner according to internal relevant SOP Maintaining, updating and archiving all clinical trial files on time. Maintaining up to date knowledge of diabetes treatment, company products, and clinical trial conduction. Any other responsibilities and duties which may be required from time to time.
Bachelor’s degree of Medical science and the relevant working experience. Fluency English on both written & verbal.
Job Classification: Experienced
Primary Location: China-Guangdong-Guangzhou (Canton)
Shift: Not required
Travel: Yes, 50 % of the Time
Req ID: 1606426