Anisha Rao

Dear Hiring Manager, 

I am currently working with Alcon Laboratories Pvt.Ltd, Bangalore, India as a patient safety specialist since May-2022 and holds a total work experience of around 07 years in Drug and Device Pharmacovigilance and Clinical Trial process. I hold a Bachelor's degree in pharmacy. 

Currently, I handle trackwise data base and also have hands on experience on Argus and Arisg Safety database. 

My experience includes handling ICSR, case monitoring activities, assessment and reporting of quality and adverse event complaint records, launching required quality investigation records, scheduling expedited and perodic regulatory reports based on local and international reporting requirements. 

Additional experience includes, creation of macro-based tools for time-savings for project related reports. 

My current and previous managers can be contacted to provide more information about my ability to meet the needs of this job. I have attached a copy of my resume below for your consideration. I can be contacted at all times on the details provided below. 

Medical Device Vigilance/PV professional. Case monitoring, assessment and reporting of quality and adverse events. Submissions as per local and global regulations, guidelines, and applicable directives. Assigning event codes to the safety databases. In depth knowledge of safety databases including ARGUS, ArisG and TRACKWISE.

Bachelor's degree in pharmacy