Join Fortrea's FSP team as a Senior CRA focusing on complex cardiac monitoring and site management across Canada. Leverage your clinical monitoring skills in this engaging role that requires nationwide travel.
The Senior Clinical Research Associate II will be responsible for overseeing study site monitoring, ensuring compliance with Fortrea and regulatory standards. With a need for three or more years of experience, this role includes responsibilities like patient safety verification, data integrity maintenance, and liaising with vendors and study staff.
Key Responsibilities:
• Manage study site monitoring and completion of visits
• Ensure compliance with informed consent and regulatory guidelines
• Maintain accurate study files and prepare trip reports
• Oversee audit readiness and data quality checks
• Mentor and train junior staff in clinical operations
Requirements:
• University degree in life science or related field
• Three years of clinical monitori...