Clinical Research Associate – All Levels

• Monitor clinical trial sites through on-site and remote visits
• Build and maintain strong relationships with investigators and site staff
• Collaborate with cross-functional teams to meet project timelines
• Manage site-level study documentation, systems updates, and visit reports
• Implement corrective actions when needed to maintain study integrity
• Ensure sites are always audit- and inspection-ready

• Detail-oriented and a strong problem solver
• Highly communicative, collaborative, and adaptable
• Motivated, accountable, and able to work independently
• Positive, professional, and comfortable supporting virtual and in-person teams
• Only candidates residing in São Paulo City, Rio de Janeiro City, Curitiba, or Porto Alegre are eligible
• Must be fluent in English and Portuguese
• Bachelor’s degree in life sciences, pharmacy, nursing, or related field is required
• A minimum of 1 year of CRA experience required
• Must be able to travel
• Must hold a valid driver’s license

• Career growth and professional development opportunities
• Work-life balance
• Flexible working arrangements
• Collaborative and inclusive environment
• Exposure to a world of experiences and open doors
• Constant learning opportunities