Job Title: Regulatory Affairs Officer
Company: IQVIA
Location: Bengaluru, Karnataka, India (Bangalore preferred)
Job Type: Full-Time
Department: Clinical Operations
Shift: UK Shift (1:30 PM to 10:30 PM)
Keywords: Regulatory Affairs, RIMS, Regulatory Information Management System, Veeva Vault, Register, xEVMPD, Vault RIM, IDMP
Job Description:
IQVIA is seeking a Regulatory Affairs Officer to join our Clinical Operations team in Bengaluru. The ideal candidate will have hands-on experience with Veeva Vault RIM or other Regulatory Information Management Systems (RIMS), and will play a key role in maintaining data integrity and ensuring compliance with regulatory requirements.
Key Responsibilities:
- Utilize Veeva Vault RIM or RIMS (Register) applications for regulatory data management.
- Complete routine and complex data maintenance tasks according to agreed schedules.
- Ensure adherence to quality control procedures and compliance with data checklists.
- Provide training and support to users of Regulatory Information Management (RIM) systems.
- Identify and contribute to process improvements and efficiencies.
- Actively participate in business process changes and technology initiatives related to RIM.
- Collaborate with clients to support RIM system implementation and issue resolution.
- Assist in preparing for internal or client audits as required.
Preferred Companies for Experience:
Merck, GSK, TCS, Parexel
About IQVIA:
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, improving patient outcomes and population health worldwide.
