Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Safety Aggregate Report Manager

Pan India
Pan India
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)