Remote Lead Clinical Research Associate

Psi CRO; Santiago; Híbrido; CLP 71.702.000 - 105.163.000; Jornada completa

Descripción de la vacante

PSI CRO Chile is seeking a Lead Clinical Research Associate to guide the clinical team and drive trial activities at country level, with leadership, mentorship and oversight of monitoring practices. The role emphasizes remote oversight and minimal site management, focusing on overall study quality and compliance.

You will monitor timelines and patient enrollment, coordinate cross-functional teams, deliver training and reports, and support CAPA processes, site audits, and risk management across

Formación

• Minimum of 4 years’ site monitoring experience with participation in global clinical projects as a Lead Monitor.
• Experience monitoring sites in the US.
• Experience with all types of monitoring visits in Phase II and/or III.
• Strong working proficiency in English.
• Proficiency in MS Office applications.
• Ability to travel.

Responsabilidades

• Monitors project timelines, patient enrollment, data cleaning and ensuring compliance.
• Reviews monitoring visit reports for all visit types and ensures reporting compliance.
• Acts as the main communication line between Monitor, Site Management Associate, Regional Project Lead, and Project Manager.
• Leads project team calls on a country level and provides status updates and reports.
• Provides project-specific training and prepares training materials for the project team under supervision.
• Supervises source data verification and follows up on data queries at site level in the country/region.
• Ensures data integrity and compliance at a site level.
• Collaborates with investigator/site feasibility and identification process, as well as study startup.

Conocimientos

MS Office

English proficiency

Ability to travel

Educación

MD

MPharm

RN

Life Sciences degree

Descripción del empleo

PSI CRO Chile is seeking a Lead Clinical Research Associate to guide the clinical team and drive trial activities at country level, with leadership, mentorship and oversight of monitoring practices. The role emphasizes remote oversight and minimal site management, focusing on overall study quality and compliance.

You will monitor timelines and patient enrollment, coordinate cross-functional teams, deliver training and reports, and support CAPA processes, site audits, and risk management across