Global Clinical Research Site Coordinator

Psi CRO; Santiago; Híbrido; CLP 12.000.000 - 19.000.000; Jornada completa

Descripción de la vacante

Psi CRO is seeking a capable Clinical Trial Assistant to support international clinical research projects. You will streamline communication, maintain systems, and manage documents across sites and vendors.

The role requires English proficiency and prior CRO/CTA experience, with responsibilities spanning CTMS, ISF, regulatory submissions, and study material logistics. Join a global team and advance your career in clinical research.

Formación

• College/University Degree in Life Sciences.
• Administrative experience in international settings.
• Prior CTA experience for CROs.
• Experience in Clinical Research.
• Knowledge of local regulations.
• Fluent in English.
• Proficient with MS Office.
• Ability to plan and work in a dynamic team.
• Excellent communication and collaboration.

Responsabilidades

• Be the main point of contact between site personnel and CRA; assist with queries and EDC completion.
• Act as the primary site contact for vendors, study supplies and access management.
• Ensure pre-study testing (scans, MRI/CT forms, ECGs) is completed at sites.
• Assist Monitors in CTMS data entry; track issue resolution and actions.
• Manage order, receipt, inventory, distribution, return/recall and reconciliation of supplies.
• Ensure regulatory submissions and ethics notifications are up to date.
• Coordinate site, TMF, and systems audits and inspections.
• Manage TMF at site/country level; file ISF and ISF checklists.
• Arrange and track training for site teams in vendor systems.
• Review document management and translation status for the study.
• Ensure safety information flow with investigative sites.

Conocimientos

Communication skills

Team collaboration

English proficiency

MS Office proficiency

Planning ability

Educación

College/University Degree in Life Sciences

Herramientas

MS Office

Descripción del empleo

Psi CRO is seeking a capable Clinical Trial Assistant to support international clinical research projects. You will streamline communication, maintain systems, and manage documents across sites and vendors.

The role requires English proficiency and prior CRO/CTA experience, with responsibilities spanning CTMS, ISF, regulatory submissions, and study material logistics. Join a global team and advance your career in clinical research.