Clinical Data Coordinator I supports data review activities for clinical research protocols, ensuring data integrity standards are met. The role involves routine clinical data reviews, documentation maintenance, and collaboration with the Clinical Data Science team on low to medium complexity projects across Mexico City and Colombia.
Responsibilities
Perform routine clinical and third-party data reviews for enrolled study subjects
Maintain clinical data management study documentation as needed
Execute data review and analytics for low to medium complexity assignments
Manage third-party data reconciliation processes
Support Clinical Data Science Lead with eCRF and data validation specification development
Requirements
1-2 years clinical data management experience in CRO or pharmaceutical company
Basic knowledge of drug development process
Proficiency with at least one Clinical Data Management System (Medidata RAVE, InForm, Veeva)
Strong computerized information systems and MS Office skills
Excellent written and oral communication abilities
Bachelor's degree or local equivalent
Fluent English and host country language proficiency

📌 Clinical Data Coordinator I (Xico)
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📍 Xico