IQVIA has announced openings for the position of Analyst โ Regulatory Intelligence in Bangalore, India. This opportunity is ideal for experienced professionals with expertise in Drug Safety, Pharmacovigilance, Regulatory Affairs, ICSR submissions, Periodic Safety Reports, Risk Management Plans (RMP), Signal Detection, and Regulatory Intelligence.
The role involves monitoring global regulatory updates, preparing high-quality regulatory intelligence content, and supporting pharmaceutical and medical device companies with critical regulatory information across the USA, Canada, APAC, and international markets.
Professionals looking for IQVIA Regulatory Intelligence Jobs 2026, Drug Safety Jobs in Bangalore, Pharmacovigilance Jobs, or Regulatory Affairs Careers should consider this opportunity.
About IQVIA Regulatory Intelligence
IQVIA Regulatory Intelligence provides real-time regulatory information from more than 110 countries, regions, and international organizations. The platform helps pharmaceutical and medical device companies stay compliant by delivering:
- Global regulatory intelligence
- Drug safety guidance
- Pharmacovigilance updates
- Clinical trial regulations
- Regulatory document summaries
- Country-specific regulatory requirements
- Timely compliance alerts
Job Details
| Particular | Details |
|---|---|
| Position | Analyst โ Regulatory Intelligence |
| Company | IQVIA |
| Job Location | Bangalore, India |
| Job Type | Full-Time |
| Department | Regulatory Intelligence |
| Experience | 3โ4 Years |
| Qualification | Master’s Degree in Pharmacy or Life Sciences |
| Industry | Clinical Research / Pharmacovigilance / Regulatory Affairs |
| Application Deadline | July 1, 2026 |
Key Responsibilities
The selected candidate will be responsible for:
- Preparing and maintaining regulatory intelligence documents related to Drug Safety and Pharmacovigilance.
- Monitoring regulatory updates issued by health authorities across APAC, USA, and Canada.
- Reviewing laws, guidance documents, regulations, and technical requirements.
- Supporting clinical trial regulatory intelligence activities.
- Performing quality control of regulatory content prepared by external experts.
- Assisting customers and internal teams with regulatory knowledge.
- Acting as a subject matter expert for Drug Safety regulations.
- Supporting regulatory submissions and compliance activities.
- Collaborating with global cross-functional teams.
- Conducting internal regulatory knowledge-sharing and training sessions.
- Improving regulatory intelligence processes and maintaining quality standards.
Required Qualifications
Applicants should possess:
- Master’s Degree in Pharmacy or Life Sciences
- 3โ4 years of Regulatory Affairs or Pharmacovigilance experience
- Experience with global Drug Safety submissions
- Knowledge of USA, Canada, and APAC regulations
- Excellent written and verbal communication skills
- Strong analytical and documentation abilities
- Attention to detail and quality-focused mindset
- Ability to work in a fast-paced global environment
Preferred Skills
Candidates with experience in the following areas will have an advantage:
- Individual Case Safety Reports (ICSR)
- Periodic Safety Reports
- Risk Management Plans (RMP)
- Signal Detection
- Literature Review
- Regulatory Intelligence
- Regulatory Impact Assessment
- Clinical Trial Regulations
- Quality Management Systems
- Microsoft Office Suite
- AI-powered document summarization tools such as Microsoft Copilot
- Cross-functional collaboration
- Regulatory documentation review
Knowledge Required
Ideal candidates should have expertise in:
- Pharmacovigilance Regulations
- Drug Safety Compliance
- Adverse Event Reporting
- Regulatory Authority Requirements
- ICSR Submission Timelines
- Periodic Safety Reporting
- Ethics Committee Reporting
- Global Regulatory Intelligence
- Regulatory Trend Analysis
- Regulatory Documentation
Why Join IQVIA?
IQVIA is one of the world’s leading healthcare intelligence and clinical research organizations. Employees benefit from:
- Global career opportunities
- Exposure to international regulatory agencies
- Collaborative work environment
- Continuous learning and professional development
- Opportunity to work on cutting-edge regulatory intelligence projects
- Strong focus on innovation and digital transformation
- Stable career growth in Regulatory Affairs and Pharmacovigilance
Estimated Salary
Based on current market trends for similar Regulatory Intelligence roles in India, the expected annual salary is approximately:
โน8,00,000 โ โน14,00,000 per annum (CTC)
Actual compensation depends on experience, skills, and interview performance.
How to Apply
