Clinical Research Associate II/III

Job Description:• Designing and analyzing clinical trials and interpreting complex medical data to contribute to treatment development• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process• Collaborating with investigators and site staff to facilitate smooth study conduct• Performing data review and resolution of queries to maintain high-quality clinical data• Contributing to the preparation and review of study documentation, including protocols and clinical study reportsRequirements:• Bachelor’s degree in a scientific or healthcare-related field• Minimum of 2 years of experience as a Clinical Research Associate• 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• Ability to travel at least 60% of the time (international and domestic - fly and drive)• Possess a valid driver’s licenseBenefits:• In addition to your competitive salary, ICON offers a range of additional benefits focused on well-being and work life balance 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 maximize 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 Apply tot his job