Clinical Research Associate I

• Coordinate all activities for setting up and monitoring a study
• Complete accurate study status reports and maintain study documentation
• Run sponsor-generated queries efficiently
• Take responsibility for study cost efficiency
• Participate in the preparation and review of study documentation and feasibility studies for new proposals as required
• Develop and maintain collaborative relationships with key stakeholders, clinical investigators, and site staff
• Ensure patient safety and compliance with ICON's procedures, protocols, and regulatory requirements

• University degree in medicine, science, or equivalent
• Relevant clinical trial monitoring experience
• Knowledge of ICH-GCP guidelines
• Expertise to review and evaluate medical data
• Excellent written and verbal communication in English
• Good social skills enabling you to deal with queries in a timely manner
• Willingness to travel as required (approximately 60%)
• Legal right to work in Brazil

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways