{"id":4133718,"url":"https://alion.io/job/icon-cra-ii-27","title":"CRA II","company":{"id":5677,"name":"ICON","domain":"iconplc.com","url":"https://alion.io/company/icon","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":86,"open_postings":59,"ghost_share":0,"stale_share":0.763,"repost_share":0.017,"time_to_fill_p50_days":19,"computed_at":"2026-11-11T05:49:22Z"}},"role":"Biotech","role_family":"Biotech","seniority":"middle","employment_type":"full_time","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"board_field","remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Burlington, Canada"],"countries":["CA"],"hiring_countries":["CA"],"hiring_countries_total":1,"salary":null,"salary_estimate":null,"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Good Clinical Practice","optional":false}],"status":"live","first_seen_at":"2026-11-11T00:00:00Z","employer_posted_date":"2026-11-11","last_verified_at":"2026-11-12T03:17:06Z","board_verified":true,"closed_at":null,"days_open":1,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":1},"description":"Clinical Research Associate- Canada- TorontoAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.\nAs the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.\nAs a CRA II at ICON, you will perform site qualification, initiation, monitoring and closeout activities as assigned.\nWhat You Will Do:\nYou will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.\nKey responsibilities include:\nPerform site qualification, initiation, monitoring and closeout activities as assigned.\nVerify protocol, GCP and regulatory compliance and participant protection.\nReview source data, essential documents and site processes for accuracy and completeness.\nIdentify and follow up findings, risks and corrective actions.\nMaintain clear communication with investigators, site staff and study teams.\nRequired qualifications and experience\nRelevant life sciences, healthcare or clinical research qualification, or equivalent relevant clinical research experience.\nMinimum of 2 years of experience as a Clinical Research Associate.\nIn-depth knowledge of clinical trial processes, regulations, and ICH Good Clinical Practice (GCP) guidelines.\nKnowledge of ICH Good Clinical Practice (GCP), clinical trial conduct and site monitoring requirements.\nPractical experience with site monitoring or site management appropriate to the level of role.\nExperience performing site qualification, initiation, monitoring and closeout activities as assigned.\nExperience verifying protocol, GCP and regulatory compliance and participant protection.\nPreferred qualifications and experience\nTherapeutic area expertise relevant to assigned studies.\nExperience with risk based monitoring or centralised monitoring approaches.\nExperience with clinical trial management systems (CTMS), electronic data capture (EDC) and electronic trial master file systems.\nWorking conditions\nWillingness to travel as required (approximately 60%).\nEmployment with ICON is contingent upon having the legal right to work in the country where the role is based.\nRewards & Benefits\nICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.\nBenefits may include:\nCompetitive base salary and performance related incentives\nHealth and wellbeing programmes including medical, dental, and vision coverage where applicable\nRetirement and pension plans\nLife assurance and disability coverage\nEmployee assistance programmes and wellbeing resources\nLearning and development opportunities through structured training and career pathways\nBenefits may vary depending on role and location.\nVisit our careers site to read more about the benefits ICON offers.\nInclusion and Accessibility\nICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.\nIf you require reasonable accommodations during the recruitment process, please let us know or submit a request here.\nAre you a current ICON Employee? 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