Study Start Up Associate II at ICON

Become a crucial part of ICON’s mission as a Study Start Up Associate II, focused on clinical trial initiation. Ensure compliance and facilitate advancements in innovative therapies.
As a vital team member at ICON, this role involves regulatory document preparation, stakeholder coordination, and maintaining submission records. You will support study teams in developing essential study documents such as protocols and informed consent forms, and provide regulatory insights during start-up meetings to ensure timely study launch.
Key Responsibilities:
• Prepare and submit regulatory documents for clinical trials
• Coordinate with stakeholders for necessary study approvals
• Maintain accurate records of submissions and approvals
• Assist in developing study protocols and consent forms
• Provide regulatory input during start-up meetings
Requirements:
• Bachelor’s degree in life sciences or related field
• 1+ years’ experience in Study Start-Up
• Strong attent...