Hybrid Senior Clinical Site Coordinator — Clinical Trials

Milestone One; Buenos Aires; Híbrido; ARS 1.200.000 - 1.800.000; Jornada completa

Descripción de la vacante

Milestone One is seeking a Senior Clinical Site Coordinator to lead the preparation, activation, and daily coordination of clinical trial activities at Milestone One-supported sites in Argentina. The role requires working with investigators, hospital departments, CRAs, CTMs, and vendors with minimal supervision.

The ideal candidate has 3–5 years of direct clinical research experience, experience as a Site Coordinator, and familiarity with Phase II/III trials and start-up activities.

Formación

• University- or college-degree in life sciences, pharmacy, nursing or related field.
• 3–5 years of direct clinical research experience in a clinical environment.
• Experience as a Site Coordinator or Senior Site Coordinator.
• Experience in international Phase II or Phase III trials.
• Start-up/activation experience preferred.

Responsabilidades

• Coordinate preparation, activation, and day-to-day activities at Milestone One-supported sites in Argentina.
• Work directly with investigators, hospital departments, CRAs, CTMs, and vendors with minimal supervision.
• Establish operational processes in developing clinical research sites while operating within delegated activities.
• Support site setup, activation, screening, participant visits, monitoring, and protocol-critical periods.

Conocimientos

Site coordination

ICH-GCP

Stakeholder management

EDC systems

Fluent English (B2)

MS Office

Driver's license

Educación

Bachelor's degree in life sciences/related

Herramientas

EDC systems

MS Office

Descripción del empleo

Milestone One is seeking a Senior Clinical Site Coordinator to lead the preparation, activation, and daily coordination of clinical trial activities at Milestone One-supported sites in Argentina. The role requires working with investigators, hospital departments, CRAs, CTMs, and vendors with minimal supervision.

The ideal candidate has 3–5 years of direct clinical research experience, experience as a Site Coordinator, and familiarity with Phase II/III trials and start-up activities.