Senior Clinical Research Associate role at ICON in Mexico City overseeing clinical trial monitoring and site management. Requires extensive CRA experience with oncology background, strong regulatory knowledge, and ability to manage multiple sites independently while guiding junior staff.
Responsibilities
Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
Conduct site visits to assess performance, resolve issues, and support trial execution
Collaborate with cross-functional teams on data collection and reporting accuracy
Provide training and guidance to site staff and junior CRAs
Build and maintain relationships with site personnel and stakeholders
Requirements
Bachelor's degree in scientific or healthcare-related field
Extensive experience as Clinical Research Associate with deep trial process knowledge
Proven ability to manage multiple sites and projects simultaneously
Expertise in monitoring practices, data integrity, and site management
Proficiency in clinical trial software and tools
Strong communication and stakeholder management skills
Willingness to travel approximately 60% for site visits

📌 Sr. Cra (Xico)
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📍 Xico