Sr Clinical Data Science Lead

hace 4 semanas


Buenos Aires, Argentina ICON A tiempo completo

Sr. Clinical Data Science Lead Ecoa- Remote 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. We are currently seeking a Senior Clinical Data Science Lead to join our diverse and dynamic team. As a Senior Clinical Data Science Lead at ICON, you will play a pivotal role in leading the analysis, interpretation, and management of clinical data to drive the success of our clinical trials. You will contribute to the advancement of innovative treatments and therapies by overseeing data science initiatives and ensuring data quality and integrity across studies. What You Will Be Doing: Have good knowledge of eCOA systems and best practice of eCOA data collection. Ability to understand the eCOA build requirements documents from vendors and provide feedback to vendors. Provide feedback on both subject and site facing assessment and reports. Perform eCOA system User Acceptance Testing (both device and web applications) including review of test plans/scripts. Collaborate with cross functional teams during build design and testing. Review eCOA data and ability to troubleshoot issues for resolution. Provide data review listing, visualization, and report specification to internal teams for development and test them before production release. Communicate trends to study lead DM for follow-up actions. Provide weekly metrics reports to study DM lead and associate director. Work on multiple studies and with multiple eCOA vendor data. Attend vendor and sponsor meetings and elevate issues through escalation pathways in a timely manner. Ability to work in fast paced environments. Good communication skill and be a team player. Leading the development and implementation of clinical data management strategies to optimize data collection, analysis, and reporting. Collaborating with cross-functional teams to ensure the accurate integration of data science techniques into clinical trial designs. Overseeing the analysis of clinical data to provide actionable insights that inform study decisions and outcomes. Providing strategic guidance on data governance, quality control, and compliance with regulatory requirements. Establishing partnerships with key stakeholders to leverage the latest advancements in data science and technology in clinical research. Your Profile: Advanced degree in a relevant field such as data science, biostatistics, or life sciences. Extensive experience in clinical data science, with a strong focus on data management and analysis in clinical trials. Strong leadership skills and a proven ability to manage cross-functional teams in a fast-paced, matrix environment. Expertise in data analysis tools, statistical software, and data visualization techniques. Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive change in a complex organization. Nous recherchons actuellement un Senior Clinical Data Science Lead pour rejoindre notre équipe diversifiée et dynamique. En tant que Senior Clinical Data Science Lead chez ICON, vous jouerez un rôle essentiel dans la direction de l’analyse, de l’interprétation et de la gestion des données cliniques afin de soutenir la réussite de nos essais cliniques. Vous contribuerez à l’avancement de traitements et thérapies innovants en supervisant les initiatives de data science et en garantissant la qualité et l’intégrité des données à travers les études. Ce que vous ferez : Posséder une bonne connaissance des systèmes eCOA et des meilleures pratiques de collecte de données eCOA. Être capable de comprendre les documents de spécifications pour la configuration eCOA fournis par les prestataires et leur fournir un feedback pertinent. Fournir des retours sur les évaluations et rapports destinés aux sujets et aux sites. Effectuer les tests d’acceptation utilisateur (UAT) des systèmes eCOA (applications web et appareils), y compris la révision des plans et scripts de test. Collaborer avec des équipes transversales lors de la conception et des phases de test des configurations. Examiner les données eCOA et être capable d’identifier et résoudre les problèmes éventuels. Fournir aux équipes internes des spécifications pour les listings de revue des données, les visualisations et les rapports, puis tester ces éléments avant leur mise en production. Communiquer les tendances au Data Manager (DM) responsable de l’étude pour les actions de suivi. Fournir des rapports hebdomadaires de métriques au responsable DM de l’étude et à l’associate director. Travailler sur plusieurs études et avec plusieurs prestataires eCOA. Participer aux réunions avec les prestataires et les sponsors et escalader les problèmes via les voies d’escalade appropriées en temps opportun. Être capable de travailler dans un environnement dynamique et exigeant. Disposer de bonnes compétences en communication et avoir un esprit d’équipe. Diriger le développement et la mise en œuvre de stratégies de gestion des données cliniques afin d’optimiser la collecte, l’analyse et le reporting des données. Collaborer avec des équipes transversales pour garantir l’intégration précise des techniques de data science dans les plans d’essais cliniques. Superviser l’analyse des données cliniques afin de fournir des informations exploitables pour soutenir les décisions et résultats des études. Fournir des conseils stratégiques sur la gouvernance des données, le contrôle qualité et la conformité réglementaire. Établir des partenariats avec des parties prenantes clés afin de tirer parti des avancées les plus récentes en data science et en technologies appliquées à la recherche clinique. Votre profil : Diplôme avancé dans un domaine pertinent tel que la data science, la biostatistique ou les sciences de la vie. Expérience approfondie en data science clinique, avec un fort accent sur la gestion et l’analyse des données dans les essais cliniques. Solides compétences en leadership et capacité démontrée à gérer des équipes transversales dans un environnement dynamique et matriciel. Expertise dans les outils d’analyse de données, logiciels statistiques et techniques de visualisation. Excellentes compétences en communication, relations interpersonnelles et gestion des parties prenantes, avec la capacité d’influencer et de conduire le changement dans une organisation complexe 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. 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. 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 to apply #J-18808-Ljbffr



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