Senior Clinical Research Associate

ppICON 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. /ppWe are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. /ph3Responsibilities /h3ulliMonitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. /liliConducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. /liliCollaborating with cross-functional teams to ensure timely and accurate data collection and reporting. /liliProviding training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. /liliBuilding and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. /li /ulh3Your Profile /h3ulliAdvanced degree in a relevant field such as life sciences, nursing, or medicine. /liliExtensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. /liliProven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills. /liliExpertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. /liliExcellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. /liliAbility to travel at least 60% of the time (international and domestic) and should possess a valid driver’s license. /liliLocation: Rome, Venice or Florence. /li /ulh3What ICON Can Offer You /h3ulliCompetitive salary and a range of benefits designed to support well-being and work-life balance. /liliVarious annual leave entitlements and health insurance offerings to suit you and your family’s needs. /liliCompetitive retirement planning offerings to maximize savings. /liliGlobal Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of professionals for well-being support. /liliLife assurance and flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, and health assessments. /li /ulpVisit our careers site to read more about the benefits ICON offers. /ppAt 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. /ppIf, 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. /ppInterested 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. /ppAre you a current ICON Employee? Please click here to apply /p /p #J-18808-Ljbffr