Senior CRA / CRA II - Home-Based (CAN) ICON plc is a world-leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Overview ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. DESCRIPTION DU POSTE ICON plc est une organisation de recherche clinique et dintelligence en soins de sant de premier plan lchelle mondiale. De la molcule la mdecine, nous faisons progresser la recherche clinique en offrant des services externaliss aux entreprises pharmaceutiques, biotechnologiques et dquipement mdical, ainsi quaux organismes gouvernementaux et de sant publique. En maintenant nos patients au centre de toutes nos activits, nous aidons acclrer le dveloppement des mdicaments et des dispositifs qui sauvent des vies et amliorent la qualit de vie. Nos employs sont au cur de notre culture et constituent la force motrice de notre succs. Les employs dICON ont pour mission de russir et leur passion garantit que nous faisons bien notre travail. Responsibilities As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements. Responsabilits En tant quassoci(e) de recherche clinique (ARC), vous surveillerez les progrs des tudes cliniques aux centres dtude ou distance, et vous vous assurerez que les tudes cliniques sont menes, documentes et signales conformment au protocole, aux procdures oprationnelles normalises (PON), aux bonnes pratiques cliniques (BPC) labores par la Confrence internationale sur lharmonisation (CIH) et toutes les exigences rglementaires applicables. Qualifications What do you need to have? Undergraduate degree or its international equivalent in clinical, science, or health related field from an accredited institution; a licensed healthcare professional (i.e., registered nurse); or equivalent work experience required 1+ years of clinical monitoring experience or equivalent combination of education and experience is required for the level 2 role; 3+ years is required for a level 3 ONCOLOGY MONITORING EXPERIENCE PREFERRED ABILITY TO TRAVEL 70% Knowledge of ICH and local regulatory authority regulations regarding drug trials To qualify, applicants must be legally authorized to work in the United States or Canada, and should not require, now or in the future, sponsorship for employment visa status. Benefits of Working in ICON Our success depends on the knowledge, capabilities and quality of our people. Thats why we are committed to developing our employees in a continuous learning culture one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, 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. Qualifications Que devez-vous avoir? Avoir un baccalaurat ou son quivalent international dans un domaine clinique, scientifique ou li la sant dun tablissement accrdit; tre un professionnel de la sant autoris (c.--d., une infirmire diplme); ou avoir une exprience de travail quivalente Un minimum de 1ans dexprience en surveillance clinique ou une combinaison quivalente dducation et dexprience pour le rle de niveau2; plus de 3ans pour le rle de niveau3 BILINGUE (ANGLAIS/FRANAIS) REQUIS EXPRIENCE DE SUIVI EN ONCOLOGIE PRFRABLE CAPACIT DE VOYAGER DE 70% Connaissance des rgles de la CIH et des autorits de rglementation locales relatives aux tudes sur les mdicaments Pour tre admissibles, les candidats doivent tre lgalement autoriss travailler aux tats-Unis ou au Canada, et ne doivent pas avoir besoin de parrainage pour leur visa demploi maintenant ou lavenir. Les avantages de travailler pour ICON Notre succs dpend des connaissances, des capacits et de la qualit de nos employs. Cest pourquoi nous nous engageons dvelopper nos employs laide dune culture dapprentissage continu une culture o nous vous mettons au dfi de travailler avec engagement et o chaque exprience contribue votre dveloppement professionnel. Chez ICON, notre objectif est de vous fournir une gamme complte et comptitive de rcompenses comprenant, non seulement un excellent salaire de base, mais aussi un large ventail de programmes de rmunration et de reconnaissances. De plus, nous offrons des avantages sociaux, des politiques de soutien et des initiatives de bien-tre de premire qualit, afin de vous soutenir, vous et votre famille, toutes les tapes de votre carrire, maintenant et lavenir. ICON, y compris ses filiales, est un employeur inclusif qui offre des chances gales demploi et qui sengage offrir un milieu de travail exempt de discrimination et de harclement. Tous les candidats qualifis recevront une considration gale pour lemploi sans gard la race, la couleur, la religion, le sexe, lorientation sexuelle, lidentit de genre, lorigine nationale, le handicap ou le statut dancien combattant protg. Si, en raison dun problme de sant ou dun handicap, vous avez besoin dun accommodement raisonnable pour toute partie du processus de candidature, ou afin dexcuter les fonctions essentielles dun poste, veuillez nous en aviser. #LI-REMOTE 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 maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. 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, color, 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 or submit a request here. 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. Are you a current ICON Employee? Please click here to apply. #J-18808-Ljbffr
Job Title
Senior Clinical Research Associate