Clinical Trial Site Activation Lead

Swiss Medical Group; Partido de Quilmes; Presencial; ARS 90.595.000 - 135.892.000; Jornada completa

Descripción de la vacante

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence. Direct and manage the delivery of site activation, maintenance and regulatory activities for studies, ensuring timelines and budgets are met.

You will coordinate with Regulatory & Site Activation across regions to deliver the agreed scope and maintain CTMS data with high quality. Join a team that supports feasibility assessments, site lists, and collaboration with investigators,

Formación

• Bachelor's degree in life sciences or related field required.
• 7+ years of relevant experience in scientific or clinical environment.
• Strong knowledge of GCP/ICH guidelines and regulatory requirements.
• Excellent communication and negotiation skills; ability to lead cross-functional teams.
• Proven ability to manage multiple projects with high quality and deadlines.

Responsabilidades

• Coordinate site activation/maintenance activities per project plan.
• Review regulatory documents and manage eTMF/CTMS data.
• Support regulatory submissions and site/start-up processes.
• Maintain relationships with sponsors, sites and internal stakeholders.

Conocimientos

Regulatory Knowledge

Project Management

GCP/ICH Knowledge

Communication

Leadership

Educación

Bachelor's degree Life sciences or related field

Herramientas

MS Office

CTMS

Clinical trial databases

Descripción del empleo

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence. Direct and manage the delivery of site activation, maintenance and regulatory activities for studies, ensuring timelines and budgets are met.

You will coordinate with Regulatory & Site Activation across regions to deliver the agreed scope and maintain CTMS data with high quality. Join a team that supports feasibility assessments, site lists, and collaboration with investigators,