CRA I or CRA II – São Paulo Responsibilities Coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. Run sponsor‑generated queries efficiently and ensure study cost efficiency; participate in the preparation and review of study documentation and feasibility studies for new proposals. Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff. Ensure patient safety by complying with ICON’s procedures, protocols, and regulatory requirements. Qualifications University degree in medicine, science, or equivalent. Knowledge of ICH‑GCP guidelines and ability to review and evaluate medical data. Excellent written and verbal communication in English. Good social skills to handle queries in a timely manner. Ability to travel at least 60% of the time (international and domestic – fly and drive) and hold a valid driver’s licence. Benefits Competitive salary. Annual leave entitlements. Health insurance options to suit you and your family. Competitive retirement planning offerings. Global Employee Assistance Programme (LifeWorks) – 24‑hour access to a global network of professionals. 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 are 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, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. J-18808-Ljbffr