CRA II, Ontario - Burlington
1 month ago

Job Summary
Clinical Research Associate (CRA) role at ICON plc involves conducting site visits including evaluation initiation monitoring close out overseeing reporting conduct of clinical trials at site level maintaining solid professional relationships with site staff facilitating subject enrolment incorporating recruitment strategies action plans at site level ensuring appropriate safety reporting use online safety reporting reviewing systems such as Intralinks verifying electronic case report form data against written electronic source documentation responding to site queries escalating issues maintaining audit inspection readiness conducting IP accountability reconciliation facilitating implementation new technologies systems clinical sites maintenance study supplies.
Responsibilities
- Conduct clinical trial site visits including evaluation initiation monitoring close out
- Oversee oversee report conduct clinical trials at a site level including on-line reports updates electronic management systems
Job description
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