ICON seeks a Clinical Trial Associate based in Mexico City to support sponsor-dedicated clinical research operations. The role involves coordinating trial administration, managing documentation, and collaborating across teams to ensure protocol compliance and regulatory adherence.
Responsibilities
Coordinate and administer clinical trials while ensuring protocol and regulatory compliance
Maintain and organize clinical trial documentation and essential study files
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