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: Tempo pieno /p /p #J-*****-Ljbffr

📌 Senior Clinical Research Associate (Milano)
🏢 Icon Clinical
📍 Milano