Clinical Trial Associate role at ICON in Mexico City, offering support in clinical research operations within a sponsor-dedicated model. The position involves coordinating trial administration, managing documentation, and ensuring regulatory compliance while contributing to innovative treatment development.
Responsibilities
Coordinate and administer clinical trials while ensuring protocol and regulatory compliance
Maintain and organize clinical trial documentation including study files and regulatory submissions
Support preparation of study materials such as informed consent and case report forms
Facilitate cross-functional team communication to ensure 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
Compensation:
Competitive base salary and performance-related incentives

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