IQVIA, a global leader in clinical research and healthcare intelligence, invites talented professionals to join our mission of advancing healthcare through data-driven solutions. We are hiring a Safety Aggregate Report Specialist 1 for our Bengaluru, Karnataka facility.

This full-time, hybrid role (Job ID: R1495476) offers an exciting opportunity to contribute to pharmacovigilance and ensure patient safety worldwide.

Job Overview

Location: Bengaluru, India (Hybrid)
Job Type: Full-Time
Job ID: R1495476
Apply: Send your resume to jobs.iqvia.com

As a Safety Aggregate Report Specialist 1, you will serve as the principal owner of Safety Aggregate Report and Analytics (SARA) deliverables, ensuring compliance with service level agreements and regulatory standards.

Key Responsibilities

The role involves critical pharmacovigilance tasks to support global safety reporting. Key duties include:

Aggregate Reporting: Author and review small to medium aggregate reports, such as PBRERs, PSURs, DSURs, PADERs, ACOs, and line listings.
Signal Management: Conduct signal detection, validation, and evaluation for post-marketing and clinical trial projects; present findings in safety management teams.
Literature Surveillance: Lead or support literature reviews, identifying ICSRs and evaluating events of special interest for marketed and investigational products.
Regulatory Support: Author responses to regulatory agencies/PRAC and justification documents for labeling.
Data Analysis: Analyze and summarize safety data to identify signals, perform benefit-risk evaluations, and prepare reports for regulatory submission.
Collaboration: Interface with cross-functional teams, including Regulatory Reporting, Medical Writing, and Clinical Research, to ensure seamless project execution.
Compliance: Adhere to IQVIA and customer SOPs, participate in audits, and maintain training compliance.

Qualifications and Skills

We seek candidates with the following qualifications and skills:

Education: Bachelor’s degree (required).
Experience: 1-3 years in drug safety, aggregate reporting, signal management, or literature surveillance (preferred).
Technical Skills: Proficiency in Microsoft Office (Word, Excel, PowerPoint) and web-based applications.
Knowledge: Good understanding of medical terminology, SOPs, and pharmacovigilance regulations.
Soft Skills: Strong organizational, time management, and communication skills; ability to multitask and work independently.
Attributes: Self-motivated, detail-oriented, and adaptable to new challenges.

Why Join IQVIA?

IQVIA is a world leader in healthcare analytics, offering a dynamic environment for career growth. Benefits include:

Career Development: Opportunities to work on innovative pharmacovigilance projects.
Global Impact: Contribute to improving patient outcomes worldwide.
Flexible Work: Hybrid model with a supportive work culture rated 3.7/5 by employees.
Competitive Pay: Salaries range from ₹6.0-13.5 Lakhs annually, with top earners exceeding ₹10.1 Lakhs.

Learn more about our mission at IQVIA Careers.

How to Apply

Apply by submitting your resume at jobs.iqvia.com (Job ID: R1495476). Ensure your resume highlights relevant experience in pharmacovigilance, aggregate reporting, or signal management.

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Application Tips

Tailor Your Resume: Emphasize experience with PBRERs, DSURs, or signal detection.
Include Certifications: Attach relevant educational and professional certifications.
Research IQVIA: Understand our role in advancing healthcare solutions.

Important Disclaimer

IQVIA does not charge fees for job applications. Beware of fraudulent offers claiming to represent IQVIA. We do not use free email services like Gmail or Yahoo for official job offers. Report suspicious activities via IQVIA Contact. IQVIA is not responsible for unauthorized offers.

Why Choose a Career in Pharmacovigilance?

Pharmacovigilance is a high-demand field ensuring the safety of medicines globally. Specialists in aggregate reporting and signal management are critical to regulatory compliance and patient safety. With a growing industry, professionals skilled in PBRERs, DSURs, and data analysis are highly valued. Explore more at Pharmaceutical Journal.

Shape the Future with IQVIA

Join IQVIA in Bengaluru to advance your career in pharmacovigilance. This hybrid role offers flexibility and growth in a global organization. Apply today at IQVIA Careers or contact jobs@iqvia.com for inquiries. Let’s drive healthcare forward together

IQVIA – Hiring Safety Aggregate Report Specialist Opportunity in Bengaluru