Clinical Site Operations Coordinator

PSI CRO; Municipio de Esquel; Presencial; ARS 1.200.000 - 1.800.000; Jornada completa

Descripción de la vacante

PSI CRO is seeking an experienced Clinical Trial Administrator/CTA to support international clinical research projects in Argentina. The role focuses on site coordination, documentation management and regulatory submissions, ensuring data quality and logistics across CTMS, ISF, ISF checklists and vendor coordination.

Candidates should hold a Life Sciences degree, have experience as a CTA for CROs, and be proficient in English and MS Office.

Formación

• Degree in Life Sciences required.
• Experience as a CTA for CROs preferred.
• Experience in clinical research.
• Proficient in English and MS Office.
• Knowledge of local regulations.
• Experience in international settings is beneficial.

Responsabilidades

• Be the main point of contact between site personnel and CRA for queries and EDC completion.
• Serve as primary site contact for vendors, study supplies, and access management.
• Ensure pre-study testing of local site facilities is completed.
• Assist Monitors with CTMS data and site event information entries; track issues.
• Manage ordering, receipt, inventory storage, distribution, recall and reconciliation of clinical supplies.
• Ensure regulatory and ethics submissions and notifications are up to date.
• Coordinate site, TMF and system audits and inspections.
• Manage TMF at site and country level; file ISF and ISF checklists.
• Arrange and track site training for vendor-related systems.
• Review document management and translation status.

Conocimientos

English proficiency

Communication and collaboration skills

Team-oriented planning

Administrative work experience

Local regulations knowledge

MS Office proficiency

CTA for CROs experience

Clinical research experience

Educación

Bachelor's degree in Life Sciences

Herramientas

MS Office

Descripción del empleo

PSI CRO is seeking an experienced Clinical Trial Administrator/CTA to support international clinical research projects in Argentina. The role focuses on site coordination, documentation management and regulatory submissions, ensuring data quality and logistics across CTMS, ISF, ISF checklists and vendor coordination.

Candidates should hold a Life Sciences degree, have experience as a CTA for CROs, and be proficient in English and MS Office.