Job Description & How to Apply Below
You will play a crucial role in coordinating site activities and recruitment efforts within ICON’s global framework. This position involves collaboration with various stakeholders to ensure operational plans align with study requirements, along with oversight of vendors to achieve project milestones. Your strategic planning and risk management skills will be vital in navigating challenges during study execution.
Key Responsibilities:
• Lead management of study operations and timelines
• Directly oversee study startup and recruitment strategies
• Work collaboratively with Site Care Partners and CRA teams
• Ensure compliance with all regulatory requirements
• Address study activation escalations and resolve issues
Requirements:
• Degree in a scientific field with 3+ years experience
• Familiarity with clinical trial methodology and regulations
• Proven record of managing country level operations
• Strong problem-solving capabilities
• Excellent verbal and written communication
Apply your skills to enhance clinical study performance within ICON’s innovative environment.
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