Location
Shanghai
Job Type
Full-time
Posted
May 30, 2026
Job Description
Pharmacovigilance Reporting Associate, China
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 Reporting Associate at ICON, you will be responsible for the accurate and timely preparation of safety reports related to clinical trials and post-marketing activities.
**What You Will Do:**
You will take responsibility for pharmacovigilance and drug safety deliverables, applying your skills to ensure quality and efficiency.
Key responsibilities include:
+ Preparing and reviewing safety reports, including periodic safety updates and individual case safety reports, ensuring accuracy and compliance with regulatory standards.
+ Collecting and analyzing adverse event data from clinical trials and post-marketing ...
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 Reporting Associate at ICON, you will be responsible for the accurate and timely preparation of safety reports related to clinical trials and post-marketing activities.
**What You Will Do:**
You will take responsibility for pharmacovigilance and drug safety deliverables, applying your skills to ensure quality and efficiency.
Key responsibilities include:
+ Preparing and reviewing safety reports, including periodic safety updates and individual case safety reports, ensuring accuracy and compliance with regulatory standards.
+ Collecting and analyzing adverse event data from clinical trials and post-marketing ...
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