Clinical Research Associate

Clinical Research Associate - Oncology/Cross TA - Toronto (Field-Based)Join to apply for the Clinical Research Associate - Oncology/Cross TA - Toronto (Field-Based) role at ICON Strategic SolutionsClinical Research Associate - Oncology/Cross TA - Toronto (Field-Based)1 day ago Be among the first 25 applicantsJoin to apply for the Clinical Research Associate - Oncology/Cross TA - Toronto (Field-Based) role at ICON Strategic SolutionsGet AI-powered advice on this job and more exclusive features.As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.En tant qu’ARC (Associé(e) de recherche clinique), vous rejoindrez la plus grande et la plus complète organisation de recherche clinique au monde, propulsée par l’intelligence en santé.What You’ll Be DoingServe as the primary point of contact between investigational sites and the sponsorConduct all types of site visits, including selection, initiation, routine monitoring, and close-outEnsure site compliance with ICH-GCP, SOPs, and Health Canada regulationsMaintain up-to-date documentation in CTMS and eTMF systemsSupport and track site staff training and maintain compliance recordsMonitor patient safety, ensuring timely and accurate AE/SAE/PQC reportingSupport subject recruitment and retention efforts at the site levelOversee drug accountability and ensure proper storage, return, or destructionResolve data queries and drive timely, high-quality data entryDocument site progress and escalate risks or issues to the clinical teamAssist in tracking site budgets and ensuring timely site payments (as applicable)Collaborate with cross-functional partners including CTAs, LTMs, and CTMsCe Que Vous FerezServir de point de contact principal entre les sites d’études et le promoteurEffectuer tous les types de visites sur site, y compris la sélection, l’initiation, la surveillance de routine et la clôtureAssurer la conformité du site aux normes ICH-GCP, aux SOPs et aux règlements de Santé CanadaMaintenir la documentation à jour dans les systèmes CTMS et eTMFSoutenir et suivre la formation du personnel du site et tenir les dossiers de conformité à jourSurveiller la sécurité des patients, en assurant un signalement rapide et précis des AE/SAE/PQCAppuyer les efforts de recrutement et de rétention des participants à l’étude au niveau du siteSuperviser la gestion des médicaments, y compris leur entreposage, leur retour ou leur destruction appropriéeRésoudre les requêtes de données et encourager une saisie de données rapide et de haute qualitéDocumenter l’avancement du site et signaler tout risque ou problème à l’équipe cliniqueContribuer au suivi du budget du site et veiller aux paiements rapides (le cas échéant)Collaborer avec les partenaires interfonctionnels, incluant les CTA, LTM et CTMYou AreBased in Greater Toronto AreaEligible to work in Canada without visa sponsorshipA clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industryExperienced across multiple therapeutic areas, ideally including Oncology, Hematology, Prostate Cancer, Lung Cancer, and Early Phase/Phase 1A graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RNKnowledgeable in Health Canada regulations and working with Research Ethics Boards (REBs)Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMFA clear communicator, problem-solver, and collaborative team playerWilling and able to travel approximately 50% for on-site monitoring visitsVous ÊtesBasé(e) dans la région du Grand TorontoAutorisé(e) à travailler au Canada sans parrainage de visaUn(e) professionnel(le) de la recherche clinique avec plus de 2 ans d’expérience en surveillance sur site dans l’industrie pharmaceutique ou auprès d’une CROExpérimenté(e) dans plusieurs aires thérapeutiques, idéalement en oncologie, hématologie, cancer de la prostate, cancer du poumon et en phases précoces / Phase 1Titulaire d’un baccalauréat en sciences de la vie ou d’un diplôme équivalent, ou infirmier(ère) autorisé(e) (IA)Connaissant bien les règlements de Santé Canada et le travail avec les comités d’éthique de la recherche (CER)Maîtrisant les ICH-GCP, les exigences réglementaires locales et les systèmes cliniques comme le CTMS et le eTMFUn(e) communicateur(trice) clair(e), apte à résoudre des problèmes et collaboratif(ve) au sein d’une équipePrêt(e) et capable de voyager environ 50 % du temps pour des visites de surveillance sur siteWhat ICON Can Offer YouOur success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.Our Benefits Examples IncludeVarious annual leave entitlementsA range of health insurance offerings to suit you and your family’s needsCompetitive retirement planning offerings to maximise savings and plan with confidence for the years aheadGlobal Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-beingLife assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among othersVisit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefitsAt ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.https://careers.iconplc.com/reasonable-accommodationsInterested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.Seniority levelSeniority levelEntry levelEmployment typeEmployment typeFull-timeJob functionJob functionResearch, Analyst, and Information TechnologyIndustriesPharmaceutical ManufacturingReferrals increase your chances of interviewing at ICON Strategic Solutions by 2xSign in to set job alerts for “Clinical Research Associate” roles.Research Coordinator I Dialysis ResearchResearch Assistant I Spine Surgery Rsrch GroupResearch Assistant (SRI) - Evaluative Clinical Sciences - Casual 2025-14659 (2025-14659)Research Associate (SRI) - Evaluative Clinical Sciences - Temporary Full-time 2025-14160 (2025-14160)Research Assistant (SRI) - Evaluative Clinical Sciences - Casual - 2025-14669 (2025-14669)Research Assistant (SRI) - Evaluative Clinical Sciences - Regular Part-time 2025-14133 (2025-14133)Research Assistant (SRI) - Evaluative Clinical Sciences - Regular Full-time 2025-13686 (2025-13686)Research Assistant (SRI) - Evaluative Clinical Sciences - Regular Full-time 2025-14055 (2025-14055)Clinical Research Assistant (SRI) - Evaluative Clinical Sciences - Regular Full-time 2025-14379 (2025-14379)Research Coordinator III - Women's Age LabClinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-time 2025-14162 (2025-14162)Research Assistant I MAP Centre for Urban Health SolutionsResearch Assistant (SRI) - Evaluative Clinical Sciences - Temporary Part-Time - 2025-14642 (2025-14642)Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-time 2025-14269 (2025-14269)Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-time 2025-14159 (2025-14159)We’re unlocking community knowledge in a new way. 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