500880 Drug Safety Associate
Clinical Careers Page(1 month ago)
About this role
A Drug Safety Associate at ICON supports safety monitoring of investigational drugs within clinical research programs, contributing to the evaluation and reporting of adverse events. The role operates within a global clinical research environment to support the development and delivery of safe therapies through accurate safety data management and regulatory reporting.
Required Skills
- Adverse Events
- Event Coding
- Safety Reporting
- Database Management
- Regulatory Knowledge
- Detail Orientation
- Communication
- Organization
- Collaboration
Qualifications
- Bachelor's Degree in Scientific or Healthcare Field
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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