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⏰ Full-time

Senior Pharmacovigilance Reporting Associate

ICON Clinical Research
Location πŸ“ Chennai, India
Posted πŸ“… June 22, 2026
Work Type ⏰ Full-time

Position Overview

Senior Pharmacovigilance Reporting Associate (Must Have: Safety Submission experience)

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 Senior Pharmacovigilance Reporting Associate at ICON, you will be essential in ensuring accurate and timely reporting of safety data related to pharmaceutical products.

**What You Will Do:**

Your experience in pharmacovigilance and drug safety will be key in delivering high-quality outcomes and mentoring colleagues.

Key responsibilities include:

+ Preparing and submitting adverse event reports and safety data in accordance with regulatory requirements and internal policies, ensuring accuracy and completeness.
+ Collaborating with clinical and regulatory teams to review and analyze saf...

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Job Details

⏰
Employment Type
Full-time
πŸ“Š
Category
other-general
🏠
Work Arrangement
On-site
πŸ“
Location
Chennai, India