Clinical Research Associate

📋 Description

• Perform and coordinate assigned clinical monitoring activities in accordance with ICH-GCP
• Conduct pre-study, initiation, interim monitoring, and closeout visits as required, assessing
• Build and maintain collaborative relationships with investigators, site personnel, study vendors
• Provide protocol-specific and study-related training to assigned clinical sites and participate in
• Maintain oversight of site performance by monitoring enrollment, CRF data entry, protocol deviation
• Communicate site performance, risks, issues, and progress to the Clinical Study Team and

🎯 Requirements

• Bachelor’s degree in a relevant scientific discipline, with at least 2 years of relevant Clinical
• Experience supporting global oncology trials is preferred, as is experience within the
• Thorough understanding of clinical trial processes, ICH-GCP principles, and associated regulatory
• Experience with clinical site monitoring, compliance assessment, site management, clinical
• Strong communication and interpersonal skills, with the ability to establish productive
• Excellent organizational and prioritization abilities, with the capacity to manage multiple

🎁 Benefits

• Hybrid working arrangement based in São Paulo.
• Opportunity to contribute to clinical research programs focused on advancing treatments for
• Exposure to global clinical trials and pharmaceutical/biotechnology research environments.
• Opportunities to develop expertise in clinical monitoring, study management, regulatory compliance
• Opportunities to mentor and support less experienced clinical research professionals.
• Collaboration with multidisciplinary and international clinical study teams.