Pharmacovigilance Reporting Associate

ICON plc

26 days ago

Taiwan

Hybrid

Full Time

Junior

0 applicants

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About this role

ICON plc is seeking a Pharmacovigilance Reporting Associate to join their team. The role involves ensuring the accurate and timely preparation of safety reports related to clinical trials and post-marketing activities, while maintaining compliance with regulatory requirements.

Skills

Qualifications

Bachelor’s degree in life sciences, pharmacy, or a related field

About ICON plc

iconplc.com

ICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.