CRA II, Ontario
Clinical Careers Page(1 month ago)
About this role
A Clinical Research Associate II (CRA II) at ICON plc is a mid-level clinical research professional based remotely in Ontario within a global healthcare intelligence and clinical research organization. The role supports clinical trial operations and site interactions while ensuring adherence to regulatory standards and contributing to operational excellence across studies.
Required Skills
- Clinical Monitoring
- Site Management
- Regulatory Compliance
- ICH-GCP
- EDC
- Safety Reporting
- Audit Readiness
- Communication Skills
- IP Accountability
- Travel Flexibility
Qualifications
- BA/BS/BSc
- Bachelor's Degree in Science
- Registered Nurse (RN)
- Full Driver's License
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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