Senior Clinical Research Associate (Brazil)

📋 Description

• Independently oversees all aspects of study site management to ensure patient safety is protected
• Provides guidance at the site and project level towards audit readiness standards and supports
• Establishes, updates, tracks and maintains study specific trial management tools/systems, and
• Manages site start up procedures including the feasibility and recruitment of potential
• If required, assists the negotiation of study budgets and the execution of investigator contracts
• Verifies the process of obtaining informed consent has been adequately performed and documented for

🎯 Requirements

• 4-year college degree or equivalent experience in a scientific or healthcare discipline
• 5 years or more as a CRA in either a CRO or pharmaceutical/ biotech industry or equivalent
• Significant site management experience or equivalent experience in clinical research
• Ability to communicate both verbally and in writing at the English proficiently (Professional level)
• Graduate, postgraduate degree
• Experience monitoring in rare and complex therapeutic areas