CRA I or CRA II – São Paulo

We are seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. You will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.

Responsibilities

• Work independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation.
• Run sponsor-generated queries efficiently, take responsibility for study cost efficiency, and participate in preparing and reviewing study documentation and feasibility studies for new proposals as required.
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensure patient safety by ensuring compliance with procedures, protocols, and regulatory requirements.

Qualificat...