Global Clinical Trial Manager

Worldwide Clinical Trials; Santiago; Presencial; CLP 9.000.000 - 13.000.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is seeking a capable Clinical Operations professional in Chile to lead site management across a regional portfolio. You will coordinate clinical staff, ensure site qualification, initiation, monitoring and close-out per protocol, and maintain TMF and QA standards.

The role requires a biology/health sciences degree and relevant CRO experience, with travel and strong English; Portuguese is a plus. Join a global team delivering high-quality trials across therapeutic areas.

Formación

• Four-year degree in biology, health sciences, or equivalent.
• Experience as a Senior Clinical Research Associate or CTM/LCRA.
• Travel and multi-site coordination required.
• Strong communication and collaboration capabilities.

Responsabilidades

• Lead site management activities across a geographic region.
• Coordinate a team of clinical staff to ensure quality and timeliness.
• Ensure site qualification, initiation, monitoring, and close-out per protocol.
• Maintain TMF compliance and QA standards.

Conocimientos

English proficiency

Portuguese preferred

Communication skills

Team collaboration

Project coordination

Educación

Biology/Health sciences degree (4-year)

Nursing or life sciences (2-year)

Herramientas

MS Office

eCRF

IVRS

CTMS

EDC systems

Descripción del empleo

Worldwide Clinical Trials is seeking a capable Clinical Operations professional in Chile to lead site management across a regional portfolio. You will coordinate clinical staff, ensure site qualification, initiation, monitoring and close-out per protocol, and maintain TMF and QA standards.

The role requires a biology/health sciences degree and relevant CRO experience, with travel and strong English; Portuguese is a plus. Join a global team delivering high-quality trials across therapeutic areas.