Clinical Study Assistant
ICON · Mexico City, Mexico
Clinical OperationsFull-timeCompany career page
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Role summary
ICON seeks a Clinical Study Assistant to support pharmaceutical clinical trial planning and execution in Mexico City on a remote basis. The role involves regulatory compliance, documentation review, monitoring oversight, and cross-functional collaboration with study teams and external organizations.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- 1-2 years pharmaceutical industry or clinical research organization experience
- Knowledge of global and regional regulatory compliance for clinical research
- Fluent business English, oral and written
- Strong task management and cross-functional collaboration skills
- Excellent organizational, interpersonal, and problem-solving abilities
- Willingness to travel approximately 10% as required
What you'll be doing
- Support critical day-to-day clinical study activities and regulatory inspection readiness
- Review study documentation including essential packets, protocols, and informed consent forms
- Collaborate with Clinical Operations teams, study managers, and CROs on study execution
- Support risk-based monitoring oversight and clinical trial system activities
- Assist with vendor contract administration and study close-out financial reconciliation
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.