Senior CRA at ICON Clinical Research — NeverHard

Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We're 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. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. This position is sponsor dedicated looking for someone in the GTA area. **What You Will Do:** You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include: + Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. + Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. + Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. + Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. + Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. **Your Profile:** You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience: + Bachelor's degree in a relevant scientific discipline or healthcare-related field + Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. + Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills. + Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. + Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. + Willingness to travel as required (approximately 60%) **En tant que CRA Senior chez ICON Plc** En tant que **CRA Senior (Attaché(e) de Recherche Clinique Senior)** chez ICON Plc, vous serez responsable de la supervision et de la gestion des activités liées aux essais cliniques afin de garantir leur réalisation conformément au protocole, aux exigences réglementaires et aux normes de l'industrie. Ce poste est dédié à un sponsor et s'adresse à des candidats basés dans la région du **Grand Toronto (GTA)** . **Vos responsabilités** Vous piloterez des activités de monitoring d'essais cliniques nécessitant une expertise technique approfondie, avec un fort accent sur la qualité et l'amélioration continue. **Principales responsabilités :** + Assurer le suivi des centres d'essais cliniques afin de garantir le respect des protocoles d'étude, des exigences réglementaires et des Bonnes Pratiques Cliniques (BPC/GCP). + Réaliser des visites sur site pour évaluer les performances des centres, résoudre les problématiques rencontrées et fournir le soutien nécessaire au bon déroulement des études. + Collaborer avec les équipes multidisciplinaires afin d'assurer une collecte et un reporting des données précis et réalisés dans les délais. + Former et accompagner le personnel des centres ainsi que les autres CRA afin de maintenir des standards élevés de conduite des essais cliniques. + Développer et maintenir des relations efficaces avec les équipes des centres investigateurs et les différentes parties prenantes afin de favoriser le bon déroulement des opérations cliniques. **Votre profil** Vous disposez d'une solide expérience en monitoring d'essais cliniques et êtes capable de travailler de manière autonome tout en accompagnant et guidant les autres membres de l'équipe. **Qualifications et expérience requises :** + Diplôme universitaire (Licence/Bachelor ou équivalent) dans une discipline scientifique pertinente ou dans un domaine lié à la santé. + Expérience significative en tant qu'Attaché(e) de Recherche Clinique (CRA), avec une excellente compréhension des processus d'essais cliniques et des exigences réglementaires. + Capacité démontrée à gérer simultanément plusieurs centres et projets, avec de solides compétences en organisation et en résolution de problèmes. + Expertise en monitoring, en intégrité des données et en gestion des sites, ainsi qu'une bonne maîtrise des logiciels et outils utilisés dans la recherche clinique. + Excellentes compétences en communication, en relations interpersonnelles et en gestion des parties prenantes, avec la capacité d'influencer les comportements et de promouvoir la conformité dans un environnement complexe. + Disponibilité pour des déplacements professionnels fréquents (environ **60 % du temps** ). **What ICON can offer you:** Our 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 include: + Various annual leave entitlements + A range of health insurance offerings to suit you and your family's 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 family's 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 (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers. At 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, 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 (https://careers.iconplc.com/reasonable-accommodations) Interested 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. Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply