Site Activation Partner

Site Activation Partner role at ICON involving clinical trial initiation and regulatory compliance support. The position collaborates with cross-functional teams to facilitate study start-up activities in a sponsor-dedicated model within a global clinical research organization.

Responsibilities

• Prepare and submit regulatory documentation including clinical trial applications and ethics submissions
• Coordinate approvals and authorizations with internal and external stakeholders for study initiation
• Maintain accurate records of regulatory submissions and approval status
• Support development of study documents such as protocols and informed consent forms
• Participate in study start-up meetings and provide regulatory guidance on requirements and timelines

Requirements

• Bachelor's degree in life sciences or related field
• Strong attention to detail and organizational abilities
• Excellent communication and interpersonal skills
• Ability to manage multiple concurrent tasks independently
• Clinical research or regulatory affairs experience preferred
• Willingness to travel approximately 5% as required