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Job Description & How to Apply Below
This position demands a dedicated professional with a minimum of 3 years of clinical monitoring experience, particularly within the cardiac field. You will manage site activities, ensuring compliance with all regulatory and sponsor guidelines, while leading small projects and mentoring junior staff as needed. Your insights will help in the effective execution of clinical trials.
Key Responsibilities:
• Monitor and manage all study site activities and documentation
• Ensure informed consent procedures are followed rigorously
• Conduct feasibility assessments and vendor interactions
• Prepare and present at Investigator Meetings
• Track and resolve Serious Adverse Events (SAEs) efficiently
Requirements:
• Bachelor’s degree in life sciences or equivalent experience
• Advanced skills in monitoring and site management
• Proficient computer skills with various software
• Excellent verbal and written communication abilities
• Ability to thrive in a matrix environment
Bring your cardiac trial expertise to Fortrea, enhancing the future of medical devices.
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