IQVIA Hiring 2026 – Safety Aggregate Report Specialist in Bangalore
If you are looking for opportunities in pharmacovigilance, drug safety, and clinical research, IQVIA has an opening worth considering.
IQVIA is hiring for the position of Safety Aggregate Report Spec 1 in Bangalore. The role is part of the company’s Lifecycle Safety operations and focuses on aggregate reporting, signal management, literature surveillance, and regulatory safety activities.
The position could be a good fit for life sciences professionals who already have some exposure to drug safety or pharmacovigilance and want to develop their careers with a global healthcare organization.
Job Overview
- Company: IQVIA
- Position: Safety Aggregate Report Spec 1
- Department: Lifecycle Safety / Pharmacovigilance
- Location: Bangalore, Karnataka
- Experience: 1–2 years preferred
- Qualification: Bachelor’s Degree
- Job Type: Full-time
- Application Mode: Online
- Job Requisition: R1566157
About IQVIA
IQVIA is a global healthcare and life sciences organization working across clinical research, healthcare intelligence, technology, and commercial solutions.
Its teams support pharmaceutical and biotechnology companies throughout the drug development and commercialization process. Pharmacovigilance and lifecycle safety are important parts of this work, helping organizations monitor medicine safety and meet regulatory requirements.
For professionals interested in drug safety, clinical research, and regulatory operations, IQVIA provides exposure to international projects and cross-functional teams.
About the Safety Aggregate Report Specialist Role
As a Safety Aggregate Report Spec 1, the selected professional will be involved in the preparation and management of safety deliverables for pharmaceutical products.
The position includes work related to aggregate safety reports, signal management, literature surveillance, and regulatory responses.
Candidates should be comfortable working with detailed medical information, following SOPs, managing deadlines, and maintaining high documentation standards.
Key Responsibilities
The role may involve:
- Preparing and reviewing aggregate safety reports
- Working on PBRERs and PSURs
- Supporting preparation of DSURs and PADERs
- Handling other applicable safety and device reports
- Preparing responses to regulatory agency and PRAC queries
- Conducting literature surveillance for marketed products
- Identifying relevant ICSRs and events of special interest
- Supporting signal detection and validation activities
- Preparing signal management documents and analyses
- Participating in safety management meetings
- Coordinating with clients and internal IQVIA teams
- Supporting audits, inspections, and training activities
- Tracking project metrics and reporting progress
- Following company and client SOPs
Eligibility Criteria
Candidates should have:
- A Bachelor’s Degree in a relevant discipline
- Preferably 1–2 years of experience in drug safety, aggregate reporting, signal management, or literature surveillance
- Good knowledge of medical terminology
- Understanding of SOPs and work instructions
- Good Microsoft Office skills
- Strong written and verbal communication
- Good organizational and time-management abilities
- Ability to manage multiple assignments and deadlines
- Attention to detail and accuracy
- Willingness to learn different Lifecycle Safety activities
Relevant experience in pharmacovigilance or clinical research can be particularly useful for this position.
Skills That Can Help You Get Selected
For this type of role, candidates should be familiar with areas such as:
- Pharmacovigilance
- Drug safety
- Aggregate reporting
- Signal management
- Literature surveillance
- ICSR concepts
- Medical terminology
- Regulatory safety requirements
- SOP compliance
- Microsoft Office
- Documentation and reporting
Strong communication and the ability to work independently are also important.
Important Safety Reporting Terms to Know
If you are preparing for an interview, it is useful to understand the basic purpose of common safety documents:
PBRER – Periodic Benefit-Risk Evaluation Report
PSUR – Periodic Safety Update Report
DSUR – Development Safety Update Report
PADER – Periodic Adverse Drug Experience Report
ICSR – Individual Case Safety Report
Having a clear understanding of these concepts can help candidates communicate their pharmacovigilance knowledge during the selection process.
Salary & Benefits
The job posting does not specify an exact salary figure. However, the position offers the opportunity to work in a global pharmacovigilance environment.
Potential career advantages include:
- Exposure to international safety projects
- Experience with aggregate reporting
- Learning opportunities in signal management
- Cross-functional collaboration
- Professional development and mentorship
- Career progression within Lifecycle Safety
- Exposure to global regulatory requirements
How to Apply for IQVIA Jobs
Interested candidates can apply online through the official IQVIA careers portal.
Job Title: Safety Aggregate Report Spec 1
Job Requisition: R1566157
Location: Bangalore
Candidates should submit an updated resume and ensure that their application accurately reflects their drug safety, pharmacovigilance, literature surveillance, or aggregate reporting experience.
Application Deadline: 29 August 2026
Apply as early as possible because recruitment timelines can change.
Is This a Walk-In Interview?
No.
This is an online application opportunity, and no walk-in interview has been specified for the position.
Why Consider This IQVIA Opportunity?
This role can be particularly useful for professionals who want to move deeper into pharmacovigilance and lifecycle safety.
Instead of focusing only on case processing, the position provides exposure to areas such as aggregate reports, signal management, literature surveillance, regulatory responses, and client-facing activities.
That combination can help build a broader understanding of global drug safety operations.
Quick Job Summary
| Job Detail | Information |
|---|---|
| Company | IQVIA |
| Position | Safety Aggregate Report Spec 1 |
| Location | Bangalore |
| Experience | 1–2 Years Preferred |
| Qualification | Bachelor’s Degree |
| Department | Lifecycle Safety / Pharmacovigilance |
| Job Type | Full-time |
| Job ID | R1566157 |
| Application | Online |
| Deadline | 29 August 2026 |
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the IQVIA career page.
Frequently Asked Questions
1. Who can apply for the IQVIA Safety Aggregate Report Specialist role?
Candidates with a Bachelor’s Degree and preferably 1–2 years of experience in drug safety, aggregate reporting, signal management, or literature surveillance can apply.
2. Is this a fresher job?
The posting prefers candidates with 1–2 years of relevant experience, so it is better suited to early-career professionals rather than candidates with no relevant exposure.
3. Where is the IQVIA job located?
The position is based in Bangalore, Karnataka.
4. What is the job requisition number?
The IQVIA requisition number is R1566157.
5. Is there a walk-in interview?
No. The position is being filled through the online application process.
