ICON Strategic Solutions seeks a Study Monitoring Associate II in Mexico City to support clinical trial site management and compliance. The role involves coordinating monitoring activities, ensuring regulatory adherence, and facilitating communication between sites and cross-functional teams in a sponsor-dedicated model.
Responsibilities
Coordinate monitoring activities at clinical trial sites and resolve site-related compliance issues
Prepare and review regulatory documents to ensure GCP and regulatory compliance
Collaborate with cross-functional teams to support trial sites throughout study lifecycle
Track and analyze site performance metrics, generating efficiency reports
Participate in training initiatives and mentor junior staff on clinical trial management
Requirements
Bachelor's degree in life sciences, healthcare administration, or clinical research
Clinical research, site management, or monitoring experience with GCP knowledge
Strong organizational and project management abilities across multiple priorities
Analytical skills with meticulous attention to detail and quality focus
Excellent communication and interpersonal skills for stakeholder engagement

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