Carolina Ariana Echeverria
Remote Assistant to Clinical Research Coordination @Instituto De Investigaciones Clínicas Mar Del Plata
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WORK HISTORY
Remote Assistant to Clinical Research Coordination @Instituto De Investigaciones Clínicas Mar Del Plata
IT
Support ongoing oncology trials with a focus on regulatory documentation, data entry, and trial management systems.• Manage and update Trial Master File (TMF) documents to ensure regulatory compliance and accurate record-keeping.• Perform data entry, verification, and quality control to maintain accurate study datasets.• Assist with safety reporting and preparation for monitoring visits, strengthening operational oversight skills.• Coordinate communication between investigators and study teams to maintain protocol adherence and smooth trial execution.• Utilize remote collaboration tools (Slack, Zoom, Teams, Trello, Asana) to support cross-functional study coordination.
EDUCATION
PHASE SMO/CRO
Clinical trial management training and coaching, Clinical Study Coordinator
Coderhouse
UX Writer, UX Writing
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Community Manager, Digital Marketing
Instituto Hilet
Communication and Marketing Specialisation, Marketing and Communication
Escuela de Artes Visuales Martin Malharro
Professional Illustrator, Illustration
Confederación Argentina de la Mediana Empresa (CAME)
Salary Settlements
IxDF - The Interaction Design Foundation
UX Designer, UX Design
Instituto Superior de Letras Eduardo Mallea
Proofreader and editor, Spanish literature
ABOUT CAROLINA ARIANA ECHEVERRIA
Multilingual Clinical Research professional specializing in clinical trial coordination, regulatory documentation, and patient management across oncology and multidisciplinary studies.I have supported study activities across the clinical trial lifecycle, ensuring protocol adherence, regulatory compliance (GCP), and accurate documentation. My role has involved close collaboration with investigators, site staff, and sponsors, contributing to data integrity, patient follow-up, and timely study execution.With experience in both on-site and remote research support, I have developed a strong understanding of trial documentation processes, monitoring readiness, and cross-functional coordination. My background combines operational precision with a structured, compliance-driven approach aligned with monitoring standards and trial oversight requirements.Fluent in Spanish, English, and Italian, I contribute effectively to international research environments, bringing adaptability, attention to detail, and strong cross-cultural communication to every study I support.
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