Associate Consultant null

Job Duties:

Key components of the responsibilities are as mentioned below:

• Provide application configuration expertise on Adverse Event Reporting products including Argus Safety, ArisG and related modules
• Requirements Analysis
• Development and accountability of document deliverables (Requirement Documents CBD/CS UDDs SCR Verification IQs etc.)
• Design, build and implement configuration for clients
• Conduct POCs to understand the effectiveness of the solution; incorporate feedback into the solution
• Closely work with clients to support implementation and resolve issues
• Implement Quality measures to drive operational efficiencies and articulate the value to the customer

Essentials :

• Professional experience and strong knowledge with real time experience in Drug Safety Products from Oracle/Aris Global – Argus/ArisG
• Implementation/Upgrade/Maintenance of Drug Safety Application
• Working knowledge of writing SQL queries and/or PL/SQL code
• Excellent communication and inter-personal skills
• Commitment to excellence and high quality standards
• Versatility, flexibility, and a willingness to work within changing priorities

About IQVIA

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.