IQVIA Careers 2026 | Global Data Analyst Regulatory Intelligence Bangalore

Full Time

IQVIA Careers 2026 | Global Data Analyst Regulatory Intelligence Bangalore / 20 hours ago


IQVIA Careers 2026 | Global Data Analyst Regulatory Intelligence Bangalore

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IQVIA Hiring | Global Data Analyst (Regulatory Intelligence) – Bangalore

🏢 IQVIA

📍 Bangalore, Karnataka

🎓 Any Graduate / Bachelor’s Degree

💼 1 – 2 Years (Proofreading, Technical Writing, or Editorial Experience)

🕐 Full-Time Job

Are you searching for regulatory operations jobs in Bangalore, proofreading and technical editing vacancies in clinical research, or healthcare data analyst careers at IQVIA? Leading global clinical research and healthcare technology organization IQVIA is hiring a Global Data Analyst (Regulatory Intelligence Analyst) for its Global Market Intelligence division in Bangalore.

This role focuses on post-editing machine translation workflows, performing regulatory content quality reviews, setting up Regulatory Intelligence portals, and handling client user management requests. Any graduate with 1 to 2 years of proofreading, editorial, or role management experience is eligible. To format a recruiter-ready professional resume highlighting your editorial precision, translation post-editing, and tool management skills, read our guide on how to apply for healthcare and pharma jobs online.

📋 Job Overview

  • Company: IQVIA
  • Job Title: Global Data Analyst (Regulatory Intelligence Analyst)
  • Location: Bangalore, Karnataka, India
  • Department: Global Market Intelligence (GMI)
  • Employment Type: Full-Time, Permanent
  • Experience: 1 – 2 Years (Proofreading or Editorial)
  • Qualifications: Any Graduate / Bachelor’s Degree
  • Expected Salary: ₹6.5 LPA – ₹9.5 LPA (Estimate based on profile)
  • Application Deadline: 23 July 2026

🎯 Key Responsibilities

As a Global Data Analyst for Regulatory Intelligence at IQVIA, you will:

  • Translation Workflows: Support machine translation processes and proofread/post-edit translated regulatory documents to ensure high-quality outputs.
  • Portal Management: Configure Regulatory Intelligence portals for newly onboarded clients, manage user roles, and resolve access requests.
  • Quality Review: Review regulatory text translations against source materials to maintain accuracy, compliance, and formatting.
  • Operational Reporting: Keep track of portal configurations, request resolution timelines, and report metrics to commercial and product teams.

To learn how regulatory operations careers compare against data science tracks like CDM and SAS programming in terms of salary growth, check our article on Clinical SAS vs Clinical Data Management.

🎓 Required Qualifications & Skills

Eligibility Criteria:

  • Bachelor’s degree in any discipline (Science, English Literature, Journalism, Pharmacy, etc.).
  • 1 to 2 years of professional experience in proofreading, technical writing, copy editing, or user role management.

Core Competencies:

  • Strong English proofreading skills with high attention to detail.
  • Familiarity with post-editing machine translation systems is highly preferred.
  • Basic knowledge of Regulatory Affairs or Healthcare Market Intelligence is an advantage.
  • Exceptional communication skills for coordinating with sales and product teams.

For professionals exploring global career opportunities, packages, and certification options in life sciences consulting, read our report on Healthcare Salary Trends: India vs USA.

📝 Resume Tips for IQVIA Candidates

  • Showcase Editorial Skills: Explicitly mention experience in post-editing machine translation outputs, proofreading scientific documents, or managing editorial style guides.
  • Highlight Tool Management: Detail any experience with content management systems, portals, user provisioning, or access configuration tasks.
  • Add Keywords: Integrate terms like Regulatory Intelligence, Machine Translation Post-Editing (MTPE), Quality Review, User Role Management, Technical Proofreading, and SLA adherence.

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💬 IQVIA Regulatory Intelligence Analyst Interview Questions

  • Q1. What is Machine Translation Post-Editing (MTPE) and why is it important in regulatory settings?
    Answer Guidance: MTPE is the process where humans review and refine machine-translated regulatory text. It is critical because raw machine translation can miss medical context, regulatory terminology, or formatting standards, which can lead to non-compliance when submitting dossiers to international health authorities.
  • Q2. How do you ensure high quality and accuracy when proofreading large volumes of regulatory updates?
    Answer Guidance: I use a structured checklist focusing on key regulatory attributes, cross-reference translated tables with source documents, and implement double-check protocols for critical elements like medical dosages, drug names, and compliance dates.
  • Q3. Explain how you would manage client-specific portal configurations and user access permissions.
    Answer Guidance: Portal configuration starts with mapping client requirements (such as region, therapeutic area, and roles). I follow standard operating procedures for user provisioning, assigning permissions based on the principle of least privilege, and tracking requests in a ticketing system to ensure timely resolution.

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❓ Frequently Asked Questions

Q. What is the location for this Global Data Analyst role?
This is a full-time office position based at IQVIA’s research offices in Bangalore, Karnataka, India.

Q. What is the application deadline for this IQVIA vacancy?
The official application deadline is 23 July 2026.

Q. Do I need a Pharmacy degree to apply for this job?
No. IQVIA lists Any Bachelor’s Degree as the educational qualification. Candidates with degrees in English, Science, Journalism, or other fields who have 1–2 years of proofreading or editorial experience are eligible to apply.

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