CA EmploymentAlert | Clinical Research Associate I/II - Oncology - Toronto
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Job Title


Clinical Research Associate I/II - Oncology - Toronto


Company : ICON Strategic Solutions


Location : Ontario,


Created : 2025-02-23


Job Type : Full Time


Job Description

As a CRA you will be joining the worlds largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing: Oversee multiple oncology trials, ensuring high-quality executionProvide leadership and mentorship to junior flex team membersAct as Lead SM, training and guiding other Site Managers on study protocolsDevelop essential study start-up documents, including SIV agendasRepresent Site Managers and Lead Trial Managers (LTMs) in key meetingsEnsure the SM perspective is reflected in study documents like Monitoring GuidelinesReview reports (SQV, SMV, SCV) for sites assigned to other SMs within the same trialSupport country budget development and contract negotiations in collaboration with CCS colleaguesAssist with ASV activities and ensure alignment with study objectivesMaintain compliance with Metrics/KPIs as outlined in the Quality Oversight Plan (QOP)You Are: Remote position located in Toronto Bilingual - Proficient in both written and spoken French and English.Minimum of a B.Sc., R.N., or equivalent degree, preferably in Biological SciencesAt least 2 years of experience monitoring clinical trials in the pharmaceutical industryExperience in multiple therapeutic areas is an asset, particularly in oncology (Hematology, Prostate Cancer, Lung Cancer, Early Development - Phase 1)Knowledge of risk-based/analytical monitoring approaches is an assetProficiency in clinical trial systems such as CTMS, EDC, TMF, IWRS, and safety reporting toolsAbility to actively drive patient recruitment strategies at assigned sitesStrong collaboration with investigators and site staff to meet study timelinesEffective communication and influencing skills to manage study sites effectively, both remotely and in-personAbility to work independently while being a strong collaboratorIn-depth understanding of Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirementsUp to 50% regional travel requiredTo qualify, applicants must be legally authorized to work in Canada and should not require, now or in the future, sponsorship for employment visa status.