Experience in database management and Adverse Event/Serious Adverse Event coding with MedDRA and drug coding with WHODD. Proficiency in narrative writing by extracting relevant information from the case reports/source documents. In depth knowledge of ARGUS and MEDIDATA RAVE databases. More than 3 and half years of experience working as a safety lead for multiple protocols in different therapeutic areas like interventional cardiology, peripheral intervention, cardiac rhythm management and oncology trials. Working knowledge and understanding of various adverse event reports such as SUSAR, PSURs.

Highlights:

• Coding
• Database
• Document Review
• Drafting
• Management
• Management Report
• Project Management
• Protocol
• Quality
• Clinical Management