Senior Clinical Research Associate

ppSenior Clinical Research Associate /ppICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. /ppAs a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. /ppAs 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. /ph3What You Will Do: /h3pYou will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. /ph3Key responsibilities include: /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: /h3pYou will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. /ph3Required qualifications and experience: /h3ulliBachelor's degree in a relevant scientific discipline or healthcare-related field /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. /liliWillingness to travel as required (approximately 60%) /li /ulpEmployment with ICON is contingent upon having the legal right to work in the country where the role is based. /ph3Rewards Benefits /h3pICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. /ppBenefits may include: /pulliCompetitive base salary and performance related incentives /liliHealth and wellbeing programmes including medical, dental, and vision coverage where applicable /liliRetirement and pension plans /liliLife assurance and disability coverage /liliEmployee assistance programmes and wellbeing resources /liliLearning and development opportunities through structured training and career pathways /li /ulpBenefits may vary depending on role and location. /ppVisit our careers site to read more about the benefits ICON offers. /ph3Inclusion and Accessibility /h3pICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. /ppIf you require reasonable accommodations during the recruitment process, please let us know or submit a request here. /ppSummaryLocation: Italy, Milan; Italy, RomeType: Full time /p /p #J-18808-Ljbffr