pSenior CRA /p /brpAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. /p /brpAs the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that agevolazioni patients worldwide. /p /brpAs 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. /p /brpbWhat You Will Do: /b /p /brpYou will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. /p /brpKey responsibilities include: /p /brul /brlipMonitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. /p /li /brlipConducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. /p /li /brlipCollaborating with cross-functional teams to ensure timely and accurate data collection and reporting. /p /li /brlipProviding training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. /p /li /brlipBuilding and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. /p /li /br /ul /brpbYour Profile: /b /p /brpYou will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. /p /brpRequired qualifications and experience:



/p /brul /brlipBachelor's degree in a relevant scientific discipline or healthcare-related field /p /li /brlipExtensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. /p /li /brlipProven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills. /p /li /brlipExpertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. /p /li /brlipExcellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. /p /li /brlipWillingness to travel as required (approximately 60%) /p /li /br /ul /brpbWhat ICON can offer you: /b /p /brpOur 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. /p /brpIn 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. /p /brpOur benefits examples include:



/p /brul /brlipVarious annual leave entitlements /p /li /brlipA range of health insurance offerings to suit you and your family’s needs. /p /li /brlipCompetitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. /p /li /brlipGlobal 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. /p /li /brlipLife assurance /p /li /brlipFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. /p /li /br /ul /brpVisit our careers site ( to read more about the benefits ICON offers. /p /brpAt 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. /p /brpIf, 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 ( /p /brpSalary range: €45,040.00-€56,300.00 /p #J-18808-Ljbffr

📌 Senior CRA (Italia)
🏢 Icon Clinical Research
📍 Italia