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 preparation for audit
Establishes, updates, tracks and maintains study specific trial management tools/systems
Manages site start up procedures including the feasibility and recruitment of potential investigators
Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents
Prepares for and attends Investigator Meetings and/or sponsor face-to-face meetings

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)

Senior Clinical Research Associate – Brazil

Key skills