LATAM Clinical Trial Manager: Lead Site Management

Worldwide Clinical Trials; Argentina; Presencial; ARS 1.000.000 - 1.600.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is seeking a Senior Clinical Operations professional to lead site management activities across a geographic region and ensure successful study delivery. You will coordinate CRAs, oversee site qualification, initiation, monitoring and close-out, and guarantee quality and timely deliverables in line with SOPs.

The role requires strong communication, leadership, and regulatory knowledge with travel to sites. A life sciences degree and CRO experience are preferred.

Formación

• Proven ability to lead clinical site management activities across regions.
• Strong knowledge of FDA/EU guidelines and ICH GCP.
• Experience coordinating site qualification, initiation, monitoring and close-out.
• Able to train CRAs and mentor project teams.

Responsabilidades

• Lead delivery of clinical study site management within a geographic region.
• Ensure site qualification, initiation, monitoring, and close-out per protocol and SOPs.
• Maintain quality and timeliness of clinical deliverables across assigned programs.
• Provide guidance to site management team and act as primary contact for sponsors.

Conocimientos

Interpersonal communication

Planning & organization

Presentation skills

Multitasking

Negotiation & diplomacy

Problem solving

Team leadership (remote)

Process improvement

Attention to detail

Communication in sponsor contact

Educación

Bachelor’s degree in life sciences/related field

Experience as Senior Clinical Research Associate or CTM/LCRA

Herramientas

Microsoft Office

eCRF (electronic Case Report Forms)

IVRS/IXRS

CTMS & EDC systems

Descripción del empleo

Worldwide Clinical Trials is seeking a Senior Clinical Operations professional to lead site management activities across a geographic region and ensure successful study delivery. You will coordinate CRAs, oversee site qualification, initiation, monitoring and close-out, and guarantee quality and timely deliverables in line with SOPs.

The role requires strong communication, leadership, and regulatory knowledge with travel to sites. A life sciences degree and CRO experience are preferred.