Pharmacovigilance Associate
Clinical Careers Page(17 days ago)
About this role
A Pharmacovigilance Associate at ICON plays a crucial role in monitoring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event data. The position involves ensuring compliance with regulatory standards and supporting safety-related investigations to protect patient well-being.
Required Skills
- MedDRA
- Pharmacovigilance
- Data Management
- Regulatory Compliance
- Analysis
- Argus Safety Database
- Microsoft Office
- Safety Reporting
About Clinical Careers Page
iconplc.comICON 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.
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