Senior Pharmacovigilance Specialist / Pharmacovigilance Team Leader

• Jan 2019 - Present

Pharmacovigilance Specialist

• May 2017 - Jan 2019

Managed all pharmacovigilance activities for multiple companies.Managed activities related to collecting, processing, follow up of adverse events for multiple companies.Submitted adverse events to local authority when necessary.Performed medical coding using MedDRA.Prepared PBRERs and submitted them to local authority when necessary.Performed global and local weekly literature screening for multiple companies. Performed quality control checks for ICSR reports. Performed SOP writing and updating.Translation of literatures to English.Performed adverse event training to all emloyees for multiple companies. Performed prescription approval for a controlled circulation medication. Show less

Pharmacovigilance Specialist

• Mar 2016 - Nov 2016

Managed activities related to collecting, processing, follow up of adverse events. Submitted adverse events to local authority when necessary. Performed medical coding using MedDRA. Prepared PBRERs and submitted them to local authority when necessary. Respond to medical inquiries from HCPs, patients and field staff regarding marketed products. Performed global and local weekly literature screening for all products. Performed adverse event reporting training to all company staff. Performed quality control checks for ICSR reports. Show less

Product Safety Specialist

• Nov 2014 - Mar 2016

Managed activities related to collecting, processing of adverse events. Performed actived follow up activities to adverse events. Submitted PBRERs and adverse events to local authority when necessary. Performed local weekly literature screening for all products. Performed adverse event reporting training to all company staff. Performed SOP updates based on local and global requirements. Performed adverse event reconcilation with third parties and other departments. Managed activities related to collecting, processing of adverse events. Performed actived follow up activities to adverse events. Submitted PBRERs and adverse events to local authority when necessary. Performed local weekly literature screening for all products. Performed adverse event reporting training to all company staff. Performed SOP updates based on local and global requirements. Performed adverse event reconcilation with third parties and other departments.

Intern

• Jan 2014 - Jun 2014

Intern for Pharmacovigilance Department. Intern for Pharmacovigilance Department.

Intern

• Jun 2013 - Sep 2013

Intern for Pharmacovigilance, Clinical Research and Med Info departments. Intern for Pharmacovigilance, Clinical Research and Med Info departments.

Pharmacy Intern

• Jun 2012 - Jul 2012