ICON seeks a TMF Quality Review Jr. Associate to manage Trial Master File documentation for clinical trials in a home-based Mexico City role. The position involves ensuring compliance, completeness, and accuracy of TMF records throughout trial lifecycles while collaborating with cross-functional teams.
Responsibilities
Manage Trial Master File documentation per client requirements and ICON procedures
Ensure completeness, accuracy, and timeliness of TMF records throughout trial lifecycle
Partner with cross-functional teams to collect, review, and maintain regulatory submission documents
Conduct quality checks and audits of TMF documents for regulatory and sponsor compliance
Provide guidance to internal and external stakeholders on TMF-related matters
Requirements
Minimum 3 years clinical research or document management experience in pharmaceutical/biotech/CRO
Bachelor's degree in life sciences, documentation management, or related field
Strong attention to detail and organizational skills with multitasking ability
Excellent communication and cross-functional collaboration skills
Willingness to travel approximately 5% as required
Legal right to work in Mexico

📌 Tmf Quality Review Jr. Associate (Xico)
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