ICON seeks a Senior Study Start Up Associate based in Mexico City to lead site initiation and activation activities within clinical research. The role involves feasibility assessments, regulatory submissions, and informed consent development, supporting the Study Start Up Team Lead in a home-based position.
Responsibilities
Conduct feasibility assessments and lead site identification and contract negotiations
Prepare and coordinate regulatory, ethics, and submission documentation
Develop and finalize subject information sheets and informed consent forms
Provide technical expertise and guidance to Study Start Up team leads and project teams
Requirements
Bachelor's degree or equivalent in medical or science discipline
3+ years of clinical study start-up requirements and activities experience
Fluency in Spanish and English languages
Ability to work independently and mentor team members
Willingness to travel approximately 5% as required

📌 Senior Study Start Up Associate (Xico)
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📍 Xico