Senior Clinical Research Associate (Brazil)

📋 Description

• Oversees site management to ensure patient safety and data quality.
• Guides audit readiness at site/project level and supports audits.
• Establishes and maintains trial management tools and status reports.
• Manages site start-up: feasibility, investigator recruitment, and consent.
• Conducts site visits (pre-study to close-out) and oversees monitoring.
• Documents activities and supports recruitment and data tracking.

🎯 Requirements

• 4-year college degree or equivalent in science/healthcare.
• 5+ years as CRA in CRO/pharma/biotech industry.
• Significant site management experience.
• Professional-level English communication (verbal and written).
• Experience monitoring EDC trials and EHR records.
• Knowledge of GCP/ICH guidelines and monitoring SOPs.

🎁 Benefits

• Equal Opportunity Employer; non-discrimination.
• Reasonable accommodations available for applicants with disabilities.
• Privacy policy and CA Privacy Notice referenced.