Global Clinical Trial Associate - Sponsor Dedicated, Canada Remote
Clinical Careers Page(13 days ago)
About this role
A Clinical Trial Associate at ICON supports the design, implementation, and management of clinical trials, ensuring compliance with regulatory standards and maintaining accurate documentation. The role involves coordinating study activities and collaborating with cross-functional teams to facilitate successful clinical research.
Required Skills
- clinical Trials
- Data Management
- Regulatory Compliance
- Study Coordination
- Documentation
- Healthcare
- Pharmaceutical
- Biotechnology
- Monitoring
- Data Cleaning
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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