Remote Clinical Study Coordinator – Trials Operations

ProPharma Group; Buenos Aires; Híbrido; ARS 800.000 - 1.400.000; Jornada completa

Descripción de la vacante

ProPharma Group is seeking a Central Study Coordinator to support remote site activities for assigned projects and reside in or near Buenos Aires, Argentina.

You will act as the day-to-day contact for site communications, assist with screening and recruitment, obtain medical records, re-consent participants, and manage data-entry and database monitoring in line with ICH/GCP and regulatory standards.

Formación

• Bachelor's degree or equivalent experience.
• 2+ years related experience in clinical research or coordinating sites.
• Knowledge of ICH/GCP guidelines and regulatory requirements.
• Ability to work remotely with privacy and strong communication skills.
• Multitasking, organization and attention to detail essential.

Responsabilidades

• Serve as point of contact for day-to-day Site communications and document submissions.
• Support pre-screening, screening and recruitment activities.
• Coordinate subject re-consenting, medical records, and protocol activities.
• Perform data-entry and monitor databases; respond to system queries.
• Maintain timely site communications and documentation compliant with IRB/FDA policies.
• Assist with study closeout and other site-related tasks.

Conocimientos

Communication

Data entry

IRB/FDA compliance

ICH/GCP

SOPs

Documentation

Site coordination

Remote work

Educación

Bachelor's degree

Descripción del empleo

ProPharma Group is seeking a Central Study Coordinator to support remote site activities for assigned projects and reside in or near Buenos Aires, Argentina.

You will act as the day-to-day contact for site communications, assist with screening and recruitment, obtain medical records, re-consent participants, and manage data-entry and database monitoring in line with ICH/GCP and regulatory standards.