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PHARMA JOBS POST > Regulatory Affairs > Join the IQVIA Team: Becoming a Regulatory Affairs Officer
Regulatory Affairs

Join the IQVIA Team: Becoming a Regulatory Affairs Officer

ADMIN
Last updated: September 2, 2024 1:07 pm
ADMIN 2 years ago
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IQVIA Hiring for Regulatory Affairs Officer

Contents
Regulatory Affairs OfficerJob Description

Regulatory Affairs Officer

Location: Bengaluru, India

Full time

Job Description

  • 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

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By ADMIN
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Sanyasi Pradhan, M.Pharm, is a pharma professional and entrepreneur with a strong background in the pharmaceutical industry, writing on jobs and global pharma updates
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