ICON seeks a Site Specialist II to independently manage clinical trial site operations and documentation in Mexico City. The role involves coordinating site support activities, maintaining trial metrics, and liaising with site staff to ensure study efficiency and compliance.
Responsibilities
Coordinate site-level document collection, review, and maintenance for accuracy and compliance
Serve as operational liaison addressing site staff questions on documentation, systems, and processes
Update and maintain site status, metrics, and milestones in clinical trial management tools
Support planning and logistics for site meetings, investigator meetings, and monitoring visits
Mentor junior Site Specialists and identify workflow improvements
Requirements
Bachelor's degree in life sciences, healthcare, business, or equivalent clinical research experience
Experience in site support, clinical administration, or CRO/pharma healthcare roles
Knowledge of clinical trial processes, GCP, and site documentation requirements
Strong organizational and problem-solving abilities managing multiple priorities
Excellent communication and interpersonal skills with service-focused approach
Ability to work independently and collaborate across functional teams

📌 Site Specialist Ii (Xico)
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📍 Xico