Adriana Diaz

Clinical Research Coordinator with experience in the execution and management of clinical trials at site level, including patient coordination, regulatory documentation, and compliance with national and international regulations. Experienced in regulatory submissions, protocol follow-up, and use of electronic platforms (EDC, ePRO, IRT). Strong communication with sponsors and monitors. Known for organization, attention to detail, and ability to resolve issues in high-demand environments.

Clinical Research Coordinator at Clinstile S.A. de C.V. (2020-11 – Present)

• Coordinated clinical trials in compliance with protocol and GCP
• Managed high-recruitment clinical studies
• Participated in Phase II and III clinical trials
• Coordinated patient visits (screening, follow-up, and unscheduled visits)
• Managed regulatory documentation and submissions to Ethics Committees
• Maintained direct communication with sponsors and monitors for issue resolution and study follow-up
• Worked with electronic systems: EDC, ePRO, IRT
• Coordinated biological sample shipment and follow-up with central and local laboratories
• Managed protocol deviations, adverse events, and essential documentation
• Supported audits and regulatory inspections
• Managed study kits, investigational product logistics, and visit follow-up

Clinical Research Assistant at Clinstile S.A. de C.V. (2020-09 – 2020-11)

• Supported coordinators in reviewing and maintaining regulatory binders according to protocol requirements
• Ensured accurate and up-to-date essential documentation
• Organized and maintained clinical records and study files
• Assisted with submissions to Ethics Committees and regulatory processes
• Tracked and documented protocol deviations
• Supported safety documentation, including SUSARs
• Verified consistency and integrity of regulatory documentation

Bachelor's Degree in Pharmaceutical Biology (QFB) – UNAM (2015 – 2026-06)

Diploma in Clinical Trial Monitoring – UNAM (2020-02 – 2020-09)