IQVIA Analyst Regulatory Intelligence Hiring 2026 / 4 days ago
✔ Verified by Medical Jobs India
IQVIA Hiring Analyst – Regulatory Intelligence: Bangalore & Gurugram
🏢 IQVIA
📍 Bangalore / Gurugram, India
🎓 Master’s Degree in Pharmacy or Life Sciences
💼 3 to 4 Years Experience (Drug Safety Submissions)
Are you seeking rewarding global regulatory content roles via IQVIA Careers Bangalore or Analyst Regulatory Intelligence Jobs? Leading healthcare intelligence and clinical research organization IQVIA is hiring an Analyst – Regulatory Intelligence for its offices in Bangalore and Gurugram, India.
This position requires 3 to 4 years of relevant experience in regulatory affairs, pharmacovigilance (PV), or drug safety submissions. The selected analyst will manage real-time global regulatory databases, monitor guidelines, and support safety operations. To write an optimized drug safety and compliance resume, read our guide on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | IQVIA Analytics Services Private Limited |
| Position | Analyst – Regulatory Intelligence |
| Job Locations | Bangalore (Karnataka) & Gurugram (Haryana) |
| Employment Type | Full-Time |
| Experience Required | 3 – 4 Years in Drug Safety / Regulatory Affairs |
| Qualifications | Master’s Degree in Pharmacy (M.Pharm) or Life Sciences |
| Application Deadline | July 1, 2026 |
| Estimated Salary | ₹8,00,000 – ₹14,00,000 per annum (CTC) |
| Ref ID | R1550739 |
💼 Key Responsibilities
- Prepare, review, and update regulatory intelligence documentation focusing on Drug Safety & Pharmacovigilance.
- Monitor and analyze real-time regulatory updates (including laws, guidelines, and trends) published by health authorities.
- Focus on regulatory changes across the APAC region, USA, Canada, and European markets.
- Collaborate with cross-functional internal teams and external experts to deliver timely regulatory intelligence.
- Perform quality control (QC) assessments on clinical trial regulatory content prepared by external experts.
- Provide subject matter expertise to support customer, sales, marketing, and business development inquiries.
- Act as a safety subject matter expert (SME) to help teams interpret and apply global regulatory changes.
- Deliver internal regulatory training and knowledge-sharing presentations for the RI team.
- Incorporate approved AI tools (e.g., Microsoft Copilot) to support document summarization and trend identification.
To learn how global regulatory intelligence and drug safety consultant salaries scale compared to other monitoring functions, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Experience
- Education: Master’s degree in Pharmacy (M.Pharm) or Life Sciences.
- Experience: At least 3 to 4 years of experience in drug safety, pharmacovigilance, or regulatory affairs.
- Submissions Knowledge: Hands-on experience with ICSR timelines, periodic safety report submissions, and risk management plans (RMP).
- Jurisdiction Focus: Sound knowledge of Health Authority requirements in the USA, Canada, and APAC countries.
- Analytical Aptitude: Strong ability to interpret and assess the impact of complex regulatory laws and drafts.
- Soft Skills: Excellent verbal and written communication, target-oriented planning, and organizational skills.
For pharmacy postgraduates evaluating global regulatory compliance careers against hospital or manufacturing pathways, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join IQVIA?
- IQVIA is a global leader in clinical trial execution, data solutions, and healthcare consulting.
- Gain experience in a specialized, high-growth field working with health authorities across 110+ countries.
- Structured professional development pathways into senior intelligence and consultant positions.
- Vibrant, innovative workspace utilizing advanced data analytics and AI-powered intelligence resources.
To evaluate your knowledge of GCP guidelines, protocol reviews, and clinical operations terminology, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Regulatory Intelligence vs Healthcare IT
Regulatory intelligence analysts monitor global clinical guidelines and database filings, whereas healthcare informatics supports EHR software systems. To understand these distinct careers, read our comparison on Healthcare IT vs Clinical Healthcare.
🚀 How to Apply?
Interested candidates should apply online directly on the official IQVIA Workday career portal. Click the button below to submit your application:
❓ Frequently Asked Questions
Q. What is the required experience for this Regulatory Intelligence position?
IQVIA requires at least 3 to 4 years of experience in drug safety, pharmacovigilance, or regulatory affairs.
Q. Where will this role be based?
This is a full-time role based in IQVIA’s India offices (Bangalore or Gurugram).
Q. What is the application deadline?
The Workday posting is scheduled to accept applications until July 1, 2026.