As a Clinical Research Associate II or Senior, you will play a key role in managing and supporting clinical trials from start to finish. Working remotely from São Paulo City, Rio de Janeiro City, Curitiba, or Porto Alegre, you'll conduct both on-site and remote monitoring to ensure data accuracy, regulatory compliance, and patient safety.
Key Responsibilities
- Perform regular site visits and virtual check-ins to assess protocol adherence and data quality
- Develop trusted relationships with investigators and site personnel to support smooth trial operations
- Coordinate with cross-functional teams to keep studies on track and resolve emerging issues
- Oversee site documentation, system entries, and monitoring reports to maintain audit readiness
- Identify deviations and lead corrective actions to protect study integrity
What You Bring
- Bachelor’s degree in life sciences, pharmacy, nursing, or a related discipline
- At least one year of hands-on CRA experience
- Fluency in both English and Portuguese
- Strong attention to detail, problem-solving ability, and independent work ethic
- Valid driver’s license and willingness to travel as needed
- Ability to thrive in a flexible, virtual environment while maintaining professional accountability
Why This Matters
You’ll contribute directly to the development of new medical therapies by upholding rigorous research standards. The role supports a culture rooted in empathy, inclusion, and continuous learning, where flexibility and personal growth are built into daily work. Your efforts will help keep studies inspection-ready and aligned with global regulatory expectations, advancing treatments that improve lives.
