Sr.Clinical Research Associate
Clinical Careers Page(1 day ago)
About this role
A Senior Clinical Research Associate at ICON works as a site monitor within pharmaceutical studies, managing site activities to ensure compliance with regulatory standards and study protocols. The role involves site visits, data review, and supporting study teams throughout the clinical trial phases.
Required Skills
- Veeva
- CTMS
- Risk Based Monitoring
- Source Data Verification
- Regulatory Compliance
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.
View more jobs at Clinical Careers Page →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Clinical Careers Page
Similar Jobs
FSP CRA(Tianjin)
Fortrea(1 month ago)
Manager, Clinical Research Monitoring
Edwards Lifesciences(8 days ago)
Senior Clinical Research Associate - SE region US- FSP
Parexel(1 month ago)
Clinical Research Associate II
Fortrea(3 months ago)
FSP Vaccine CRA II (Beijing）
Fortrea(1 month ago)
FSP CRA II（Shanghai）
Fortrea(1 month ago)