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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 worlds largest & most comprehensive clinical research organization, powered by healthcare intelligence.En tant quARC (Associ(e) de recherche clinique), vous rejoindrez la plus grande et la plus complte organisation de recherche clinique au monde, propulse par lintelligence en sant.What Youll 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 dtudes et le promoteurEffectuer tous les types de visites sur site, y compris la slection, linitiation, la surveillance de routine et la cltureAssurer la conformit du site aux normes ICH-GCP, aux SOPs et aux rglements de Sant CanadaMaintenir la documentation jour dans les systmes CTMS et eTMFSoutenir et suivre la formation du personnel du site et tenir les dossiers de conformit jourSurveiller la scurit des patients, en assurant un signalement rapide et prcis des AE/SAE/PQCAppuyer les efforts de recrutement et de rtention des participants ltude au niveau du siteSuperviser la gestion des mdicaments, y compris leur entreposage, leur retour ou leur destruction approprieRsoudre les requtes de donnes et encourager une saisie de donnes rapide et de haute qualitDocumenter lavancement du site et signaler tout risque ou problme lquipe cliniqueContribuer au suivi du budget du site et veiller aux paiements rapides (le cas chant)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 Bachelors 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 tesBas(e) dans la rgion du Grand TorontoAutoris(e) travailler au Canada sans parrainage de visaUn(e) professionnel(le) de la recherche clinique avec plus de 2 ans dexprience en surveillance sur site dans lindustrie pharmaceutique ou auprs dune CROExpriment(e) dans plusieurs aires thrapeutiques, idalement en oncologie, hmatologie, cancer de la prostate, cancer du poumon et en phases prcoces / Phase 1Titulaire dun baccalaurat en sciences de la vie ou dun diplme quivalent, ou infirmier(re) autoris(e) (IA)Connaissant bien les rglements de Sant Canada et le travail avec les comits dthique de la recherche (CER)Matrisant les ICH-GCP, les exigences rglementaires locales et les systmes cliniques comme le CTMS et le eTMFUn(e) communicateur(trice) clair(e), apte rsoudre des problmes et collaboratif(ve) au sein dune quipePrt(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. Thats why weve 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 familys 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 familys 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: ICON, inclusion & belonging are fundamental to our culture and values. Were 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.in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless theres every chance youre exactly what were 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)Were unlocking community knowledge in a new way. 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