As a Clinical Research Associate, you will join the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensure protocol compliance, data integrity, and patient safety throughout the trial process. Collaborate with investigators and site staff to facilitate smooth study conduct. Perform data review and resolve queries to maintain high-quality clinical data. Contribute to the preparation and review of study documentation, including protocols and clinical study reports. Qualifications: Bachelor's degree in a scientific or healthcare-related field highly preferred. Minimum of 2 years of experience as a Clinical Research Associate, with on-site monitoring experience required. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. What ICON can offer you: Our success depends on the quality of our people. We’ve built a diverse culture that rewards high performance and nurtures talent. In addition to a competitive salary, ICON offers a range of benefits focused on well-being and work-life balance for you and your family, including: Various annual leave entitlements Health insurance options to suit your needs Retirement planning options to maximize savings Global Employee Assistance Programme, TELUS Health, offering 24-hour support Life assurance Flexible country-specific benefits such as childcare vouchers, bike schemes, gym memberships, travel passes, health assessments, among others. Visit our careers website to learn more about working at ICON: At ICON, inclusion & belonging are fundamental. We are committed to providing an inclusive environment free of discrimination and harassment. If you need accommodations during the application process, please let us know through the reasonable accommodations form . Interested but unsure if you meet all requirements? We encourage you to apply regardless. You may be exactly what we're looking for, whether for this or other roles. #J-18808-Ljbffr
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