Global Clinical Trial Site Management Lead

Worldwide Clinical Trials; Ciudad de México; Presencial; MXN 600.000 - 1.000.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials in Mexico City seeks a Senior Clinical Research Associate to lead site management activities across a regional footprint. You will coordinate clinical staff, ensure site qualification, initiation, monitoring, and close-out in line with protocol and SOPs.

You will monitor data quality, TMF compliance, and risk management, while collaborating with project teams. Travel is required; strong knowledge of FDA/EU guidelines and eCRF/EDC systems is essential.

Formación

• Four-year college curriculum with a major in biological, physical or health studies.
• Alternative: nursing or life science degree (two-year program) preferred.
• Travel required and ability to work independently.

Responsabilidades

• Lead delivery of site management activities across a geographic region.
• Coordinate a team of clinical staff to ensure site qualification and initiation.
• Ensure QC and TMF readiness and regulatory compliance.
• Provide CRA training and support to project teams.
• Monitor recruitment and data quality with defined KPIs.

Conocimientos

Interpersonal communication

English language proficiency

Portuguese (preferred)

Educación

Bachelor's degree in biological/physical/health studies

Nursing or life science degree preferred

Herramientas

Microsoft Office

eCRF

IVRS

IxRS

CTMS

EDC

Descripción del empleo

Worldwide Clinical Trials in Mexico City seeks a Senior Clinical Research Associate to lead site management activities across a regional footprint. You will coordinate clinical staff, ensure site qualification, initiation, monitoring, and close-out in line with protocol and SOPs.

You will monitor data quality, TMF compliance, and risk management, while collaborating with project teams. Travel is required; strong knowledge of FDA/EU guidelines and eCRF/EDC systems is essential.