Clinical Research Associate

ppAs a CRA II at ICON, you design and analyze clinical trials, ensuring data integrity and patient safety while advancing innovative therapies. You will monitor sites, collaborate with investigators, and contribute to study documentation. This role supports cross-functional teams in a fast-paced, global environment and involves travel. You will help bring new medicines to patients faster by upholding high-quality standards and regulatory compliance. /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 /liliConduct site qualification, initiation, monitoring, and close-out visits for clinical trials /liliEnsure protocol compliance, data integrity, and patient safety throughout the trial process /liliCollaborate with investigators and site staff to facilitate smooth study conduct /liliPerform data review and resolution of queries to maintain high-quality clinical data /liliContribute to preparation and review of study documentation, including protocols and clinical study reports /liliBachelor's degree in scientific or healthcare-related field /liliMinimum of 2 years of experience as a Clinical Research Associate /liliIn-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines /liliStrong organizational and communication skills with attention to detail /liliAbility to work independently and collaboratively in a fast-paced environment /liliWillingness to travel as required (approximately 60%) /liliStrong communication /liliKnowledge of clinical trial processes and ICH-GCP /liliData review and query resolution /liliRegulatory compliance understanding /li /ulpClinical Research Associate varese, lombardia, it /p /p #J-18808-Ljbffr