Main Responsibilities
Requirements Gathering and analysis by driving/contributing to the requirements workshops
Facilitate/contribute to client demo sessions/workshops
Performs extensive testing of the application/custom code to identify/fix all issues during the testing phase

Authoring and execution of validation documents like Test scenarios, Operational and Performance Qualification scripts
Follow the cross-phase procedures and plans like Defect Management Plan, Change Control Procedure, Document Management Plan and Training Plan
Closely work with clients and vendors to support project implementation in multiple time zones
International travel readiness, work hours that overlap global client location and Time-zones
Commitment to excellence and high-quality standards
Versatility, flexibility, and a willingness to work on multiple business areas with changing priorities

Skills Required
Professional experience and strong knowledge with real time experience in Software Testing / System Implementation in the Pharmacovigilance /Life Sciences industry
Well versed with various SDLC models, Software Test life cycle and Defect Management Life Cycle
Working knowledge of writing SQL queries and/or PL/SQL code
Excellent communication and inter-personal skills
Hands on experience on any Adverse Event Reporting solutions like Argus Safety, ArisG, Oracle AERS, Clintrace and related modules will be a plus