Icon plc Hiring for Pharmacovigilance Associate Jobs 2026 Apply Online

Icon plc Hiring for Pharmacovigilance Associate Apply Online

 

Icon Plc is inviting the application for post of Pharmacovigilance Assocciate job at its Chennai and Trivandrum locations.
Candidates with hands-on experience in Clinical Trial and Post-Marketing case processing are encouraged to apply. This is an excellent opportunity for professionals seeking career growth in pharmacovigilance, drug safety, and clinical research.

Pharmacovigilance Associate

  1. Chennai, Trivandrum  JR152998
  2. Drug Safety
  3. ICON Full Service & Corporate Support
  4. Hybrid

Job Overview

ParticularsDetails
OrganizationICON plc
Job TitlePharmacovigilance Associate
DepartmentDrug Safety
Job LocationsChennai, Tamil Nadu & Trivandrum, Kerala
Reference IDJR152998
Employment TypeFull-Time
Work ModeHybrid
QualificationBachelor’s Degree in Life Sciences
ExperienceMinimum 2 Years
IndustryClinical Research & Pharmacovigilance

About the role

Pharmacovigilance Associate (Hands-on experience in Clinical Trial & Post Marketing case processing)

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

 

As a Pharmacovigilance Associate at ICON, you will monitor and ensure the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information.

Eligibility Criteria

Educational Qualification

Candidates must possess:

  • Bachelor’s Degree in Life Sciences

 

What You Will Be Doing:

  • Collect, assess, and process adverse event reports to ensure accuracy and timely compliance with regulatory requirements
  • Partner with cross-functional teams to address safety-related questions and support ongoing investigations
  • Maintain current knowledge of pharmacovigilance regulations, global safety guidelines, and industry standards
  • Manage safety inbox and acknowledge case receipt.
  • Perform case triage and book-in to safety database.
  • Enter case details accurately and write narratives.
  • Code events, drugs, and medical history using MedDRA/WHO-DD.
  • Apply correct product labeling and perform QC checks.
  • Finalize case processing and generate queries for follow-up
  • Knowledge of seriousness, expectedness, causality, and global reporting
  • Familiarity with reconciliation processes and aggregate reporting (PSUR/DSUR)
  • Ability to mentor new joiners and review SOPs
  • Working knowledge of SDEA and KPI/SLA basics
  • Process literature ICSRs and maintain compliance with monitoring requirements

 

Must Have Criteria:

  • Minimum 2 years of experience in safety background, with direct involvement in case processing
  • Solid experience in Post Marketing Surveillance/Clinical Trial case processing
  • Bachelors degree in life sciences
  • Strong analytical skills with attention to detail in data collection and reporting
  • Excellent communication and interpersonal skills, enabling effective collaboration with team members and stakeholders
  • A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities

How to Apply
Interested candidates can apply online

APPLY HERE

Frequently Asked Questions (FAQs)

1. What is the job role offered by ICON plc?

ICON plc is hiring for the position of Pharmacovigilance Associate.

2. What qualifications are required?

Candidates must hold a Bachelor’s Degree in Life Sciences.

3. How much experience is required?

A minimum of 2 years of pharmacovigilance experience is required.

4. What locations are available for this role?

The position is available in Chennai and Trivandrum.

5. Is experience in Clinical Trial case processing mandatory?

Yes, candidates should have experience in Clinical Trial and Post-Marketing case processing.

6. Is the position remote?

 

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