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Job Description & How to Apply Below
Drive excellence in clinical research as a Director, focusing on data quality and site management. Engage with regulatory affairs while enhancing data collection protocols in a collaborative environment.
In this role, you'll establish robust data collection protocols and manage relationships with clinical study partners. Bringing over five years of experience in clinical research, your leadership will be key in training teams, managing site communications, and ensuring adherence to quality standards. You will also work closely with regulatory teams to enhance our study strategies as we grow.
Key Responsibilities:
• Manage clinical site communications and data collection
• Oversee training sessions and develop training resources
• Ensure communication aligns with data collection efforts
• Contribute to regulatory filing processes and strategies
• Monitor data quality throughout the study process
Requirements:
• Minimum 5 years of managing clinical studies with FDA approval experience
• Higher education in clinical studies;
Master’s in biostats preferred
• Experience in data quality management or biostatistics
• Medical device experience is desirable
• Strong communication skills across all organization levels
Contribute to advancing clinical research with effective protocol management and data quality oversight in this vital position.
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