Sr. Clinical Research Associate

ppSr. Clinical Research AssociateICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As 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.We 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. /ph3What You Will Be Doing: /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. /li liCollaborating 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 organisational and problem-solving skills. /li liExpertise 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. /li liAbility to travel at least 60% of the time (international and domestic – fly and drive) and should possess a valid driver’s license. /li liEmployment with ICON is contingent upon having the legal right to work in the country where the role is based. /li /ulh3Rewards Benefits: /h3ulliCompetitive base salary and performance related incentives. /li liHealth and wellbeing programmes including medical, dental, and vision coverage where applicable. /li liRetirement and pension plans. /li liLife assurance and disability coverage. /li liEmployee assistance programmes and wellbeing resources. /li liLearning and development opportunities through structured training and career pathways. /li liBenefits may vary depending on role and location. /li liVisit our careers site to read more about the benefits ICON offers. /li /ulh3Inclusion and Accessibility: /h3 pICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. /p pIf you require reasonable accommodations during the recruitment process, please let us know. /p pAre you a current ICON Employee? /p pSummaryLocation: Italy, MilanType: Full time /p pSr. Clinical Research Associate • milan, lombardy, Italy /p /p #J-18808-Ljbffr