• Keyword: Regulatory Affairs, RIMS, Regulatory Information Management System, Veeva Vault, Register, xEVMPD, Vault RIM, IDMP
• Companies to look for: Merck, GSK, TCS and Parexel
• Shift: UK Shift (1:30pm to 10:30pm)
• Location: Bangalore preferred

Job Description:

1.       Hands on experience of Veeva Vault RIM or RIMS(Register) applications

2.       Completion of routine data maintenance tasks to agreed schedule

3.       Ensure defined quality control procedures are followed

4.       Ensure compliant with data checklists and defined procedures

5.       Advise, train and support users of the Regulatory Information Management (RIM) systems

6.       Recognize and Contribute areas for improvements/efficiencies in existing processes

7.       Participates as an active contributor to related business process change and technology initiatives related to RIM

8.       Closely work with clients to support implementation and resolve issues pertaining to RIM systems

9.       Completion of complex or non-routine data maintenance tasks as per the agreed schedule

10.   Support or lead the preparation of team for internal or client audits as assigned

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com