Clinical Research Associate

As a (Senior) Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Working location : Client office, flexible work from home The Senior Clinical Research Associate manages, monitors, and closes out assigned clinical trial sites, ensuring patient safety, quality execution, and compliance with laws, GCP, and sponsor standards. The role involves overseeing site operations, fostering investigator relationships, ensuring enrollment and data quality, maintaining compliance, and resolving protocol issues. The position works closely with the Site Care Partner and study team throughout site set-up, conduct, and close-out. What you will be doing: Clinical Trial Monitoring : Oversee assigned clinical trial sites from activation to database lock, ensuring compliance with laws, GCP, SOPs, and sponsor standards. Serve as primary site contact, manage site performance, monitor safety events, and resolve protocol or data issues. Conduct on-site/remote visits for initiation, monitoring, and close-out, ensuring timely documentation and Trial Master File updates. Partner with the study team to train site staff, support recruitment, ensure investigational product oversight, and maintain quality deliverables within project timelines. Clinical/Scientific and Site Monitoring Risk : Maintain in-depth knowledge of product, protocol, and therapy area to engage investigators and support clinical goals. Ensure patient safety and eligibility, provide clinical guidance, address quality events, and lead audit-related CAPA development when needed. You are: Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases Global clinical trial experience Must be fluent in English and Native Chinese speaker Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) What ICON can offer you: : Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. #J-18808-Ljbffr