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Regulatory Document Coordinator – IQVIA

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IQVIA is hiring a Senior Regulatory Document Coordinator for its Bangalore office. This full-time opportunity is ideal for candidates with a background in pharmacy, biotechnology, life sciences, or regulatory affairs who are looking to build or advance a career in regulatory documentation and submissions within a global clinical research organization.

As a Senior Regulatory Document Coordinator, you will support the preparation and coordination of regulatory documents, ensure compliance with SOPs, and collaborate with cross-functional regulatory and clinical teams.


Key Responsibilities – Senior Regulatory Document Coordinator

  • Support preparation, formatting, and compilation of regulatory documents and submissions
  • Coordinate specific regulatory documentation tasks under guidance of senior staff
  • Ensure accuracy, completeness, and compliance with applicable regulatory requirements
  • Maintain regulatory documents according to SOPs and internal quality standards
  • Provide administrative and documentation support to regulatory department staff
  • Manage multiple projects simultaneously with strong organizational skills
  • Collaborate effectively with internal teams, managers, and external stakeholders

Eligibility & Qualifications

  • Minimum High School Diploma or equivalent (mandatory)
  • Science degree preferred: Pharmacy, Biotechnology, Biology, Microbiology, or related life sciences
  • Strong interpersonal communication and organizational skills
  • Excellent proficiency in MS Word, Excel, PowerPoint, and other MS Office tools
  • High attention to detail, accuracy, and document quality
  • Basic knowledge of regulatory requirements and documentation processes
  • Ability to follow SOPs and work under supervision on multiple assignments
  • Strong teamwork and professional relationship-building skills

Why Join IQVIA? (Benefits & Growth)

  • Work with a global leader in clinical research and regulatory services
  • Exposure to international regulatory documentation and submission processes
  • Structured career growth in Regulatory Affairs & Clinical Research
  • Professional work environment with strong compliance and ethics culture
  • Competitive salary and standard IQVIA employee benefits
  • Opportunity to work on impactful healthcare and life sciences projects

Job Location

📍 Bangalore, Karnataka, India

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Salary (Estimated)

💰 ₹4,50,000 – ₹7,50,000 per annum
(Indicative range based on industry standards for similar roles in Bangalore)


Application Deadline

🗓 Valid through: March 12, 2026
(30 days from posting date unless role closes earlier)


How to Apply

Application Link

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