Instagram
youtube
Facebook

Safety Aggregate Report Manager

4–5 years
₹12 – ₹18 LPA
10 July 19, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Location: Pan India
Position: Safety Aggregate Report Manager
Experience Required: 4–5 years
Company: IQVIA

About IQVIA:
IQVIA is a global leader in human data science, dedicated to advancing healthcare through powerful analytics, transformative technology, and unparalleled domain expertise. With a mission to drive better health outcomes, IQVIA empowers innovation across the life sciences ecosystem.

Role Overview:
IQVIA is hiring for the position of Safety Aggregate Report Manager, a key role in pharmacovigilance and regulatory compliance. The ideal candidate will have a strong background in aggregate report writing or signal management and a passion for ensuring drug safety across global markets.

Key Responsibilities:

  • Prepare and review safety aggregate reports including PBRERs, DSURs, and ASRs in compliance with global regulatory standards.

  • Conduct signal detection and management activities.

  • Collaborate with cross-functional teams such as medical writers, safety physicians, and regulatory personnel.

  • Ensure high-quality documentation, accuracy, and timely submissions.

  • Stay updated on evolving pharmacovigilance regulations and contribute to process optimization.

Candidate Requirements:

  • Graduate or postgraduate degree in Life Sciences, Pharmacy, or a related field.

  • 4 to 5 years of experience in aggregate safety report writing or signal management.

  • Familiarity with global regulatory guidelines including ICH E2C, GVP modules, and MedDRA coding.

  • Strong analytical skills and attention to detail.

  • Excellent written and verbal communication abilities.

What We Offer:

  • Opportunity to work with a globally recognized leader in human data science.

  • Remote flexibility with a Pan-India hiring model.

  • Exposure to global regulatory frameworks and complex safety projects.

  • A collaborative and growth-oriented work culture.

How to Apply:
Interested candidates can send their resume to
pavan.cm@iqvia.com or apply directly via this application link.

Estimated Salary: ₹12 – ₹18 LPA (based on industry benchmarks for 4–5 years of experience in pharmacovigilance roles in India)