Study Start Up Associate I will support clinical trial initiation at ICON, managing regulatory submissions and coordinating approvals across internal and external stakeholders. The role involves preparing trial documentation, maintaining compliance records, and participating in study activation meetings from a home-based position in Mexico or Brazil.
Responsibilities
Assist in preparation and submission of regulatory documents for clinical trials
Coordinate with internal and external stakeholders to obtain study initiation approvals
Maintain accurate records of regulatory submissions and approvals
Support development of study documents including protocols and informed consent forms
Participate in study start-up meetings and advise on regulatory requirements
Requirements
Bachelor's degree in life sciences or related field
Strong attention to detail and organizational skills
Excellent communication and interpersonal abilities
Ability to manage multiple tasks independently in fast-paced environment
Willingness to travel approximately 5% as required
Legal right to work in Mexico or Brazil

📌 Study Start Up Associate I (Xico)
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📍 Xico