Senior Clinical Research Associate – Brazil

Role Overview

• 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
• Establishes, updates, tracks and maintains study specific trial management tools/systems
• Manages site start up procedures including the feasibility and recruitment of potential investigators
• Verifies the process of obtaining informed consent has been adequately performed
• Independently conducts all forms of site visits, including pre-study/qualification, initiation, routine monitoring
• Communicates effectively and proactively with both site personnel and Precision's Project and Clinical Trial Management

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, relevant experience and/or demonstrated competencies
• Significant site management experience or equivalent experience in clinical research
• Ability to communicate both verbally and in writing at the English proficiently (Professional level)

Benefits

• Health insurance
• Retirement plans
• Paid time off
• Flexible work arrangements
• Professional development opportunities