Clinical Trial Associate position supporting sponsor-dedicated clinical research operations. The role involves coordinating trial administration, managing documentation, and ensuring regulatory compliance while working with cross-functional teams in a home-based Mexico City location.
Responsibilities
Coordinate and administer clinical trials while ensuring protocol and regulatory compliance
Maintain and organize clinical trial documentation, study files, and regulatory submissions
Support preparation of study materials including informed consent and case report forms
Facilitate cross-functional team communication for smooth trial execution
Track and report clinical trial metrics and milestones
Requirements
Bachelor's degree in scientific or healthcare-related field
Prior experience or strong interest in clinical research
Knowledge of clinical trial processes, regulations, and guidelines
Excellent organizational and communication skills
Ability to work collaboratively with attention to detail
Willingness to travel approximately 10% as required
Legal right to work in Mexico

📌 Clinical Trial Associate (Xico)
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📍 Xico