Job Title

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 Solutions Clinical Research Associate - Oncology/Cross TA - Toronto (Field-Based) 1 day ago Be among the first 25 applicants Join to apply for the Clinical Research Associate - Oncology/Cross TA - Toronto (Field-Based) role at ICON Strategic Solutions Get 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 Doing Serve as the primary point of contact between investigational sites and the sponsor Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out Ensure site compliance with ICH-GCP, SOPs, and Health Canada regulations Maintain up-to-date documentation in CTMS and eTMF systems Support and track site staff training and maintain compliance records Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting Support subject recruitment and retention efforts at the site level Oversee drug accountability and ensure proper storage, return, or destruction Resolve data queries and drive timely, high-quality data entry Document site progress and escalate risks or issues to the clinical team Assist in tracking site budgets and ensuring timely site payments (as applicable) Collaborate with cross-functional partners including CTAs, LTMs, and CTMs Ce Que Vous Ferez Servir de point de contact principal entre les sites dtudes et le promoteur Effectuer tous les types de visites sur site, y compris la slection, linitiation, la surveillance de routine et la clture Assurer la conformit du site aux normes ICH-GCP, aux SOPs et aux rglements de Sant Canada Maintenir la documentation jour dans les systmes CTMS et eTMF Soutenir et suivre la formation du personnel du site et tenir les dossiers de conformit jour Surveiller la scurit des patients, en assurant un signalement rapide et prcis des AE/SAE/PQC Appuyer les efforts de recrutement et de rtention des participants ltude au niveau du site Superviser la gestion des mdicaments, y compris leur entreposage, leur retour ou leur destruction approprie Rsoudre les requtes de donnes et encourager une saisie de donnes rapide et de haute qualit Documenter lavancement du site et signaler tout risque ou problme lquipe clinique Contribuer au suivi du budget du site et veiller aux paiements rapides (le cas chant) Collaborer avec les partenaires interfonctionnels, incluant les CTA, LTM et CTM You Are Based in Greater Toronto Area Eligible to work in Canada without visa sponsorship A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry Experienced across multiple therapeutic areas, ideally including Oncology, Hematology, Prostate Cancer, Lung Cancer, and Early Phase/Phase 1 A graduate with a Bachelors degree in Life Sciences or equivalent, or a qualified RN Knowledgeable in Health Canada regulations and working with Research Ethics Boards (REBs) Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF A clear communicator, problem-solver, and collaborative team player Willing and able to travel approximately 50% for on-site monitoring visits Vous tes Bas(e) dans la rgion du Grand Toronto Autoris(e) travailler au Canada sans parrainage de visa Un(e) professionnel(le) de la recherche clinique avec plus de 2 ans dexprience en surveillance sur site dans lindustrie pharmaceutique ou auprs dune CRO Expriment(e) dans plusieurs aires thrapeutiques, idalement en oncologie, hmatologie, cancer de la prostate, cancer du poumon et en phases prcoces / Phase 1 Titulaire 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 eTMF Un(e) communicateur(trice) clair(e), apte rsoudre des problmes et collaboratif(ve) au sein dune quipe Prt(e) et capable de voyager environ 50 % du temps pour des visites de surveillance sur site What ICON Can Offer You Our 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 Include Various annual leave entitlements A range of health insurance offerings to suit you and your familys needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global 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-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: At 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. Interested 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 level Seniority level Entry level Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at ICON Strategic Solutions by 2x Sign in to set job alerts for Clinical Research Associate roles. 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