The medical review of each adverse event

The medical expertise for the local regulatory and legal dossiers

The seriousness assessment of each adverse event

Interfacing with the local Consumer Advisory Department on Post Marketing Safety requirements (trainings of Consumer Advisory Department employees)

Training of local employees on local vigilance activities and processes

Being involved in the scientific communications with health professionals (e.g. dermatologists) on the medical analysis of adverse events, product safety profile, etc. 

Interfacing with regulatory authorities on Post Marketing Surveillance issues

The reporting of adverse events to China regulatory authorities, being compliant with the regulations

Being involved in the protocol design of the clinical studies, and the evaluation of adverse events reported during clinical studies

The global post marketing safety analysis on specific formulas, and being involved in the risk management

2-5 years’ working experience in materiovigilance or pharmacovigilance is preferred

Strong interpersonal skills and team work spirit with the ability to work effectively in a matrix-type organization

Good communication skills and ability to manage difficulties

Be flexible with the ability to manage multiple projects simultaneously with minimal guidance

Excellent oral and written communication skills in both Chinese and E