Líder de Soluciones en Sitios – Ensayos Clínicos

Red Basa

Buenos Aires

On-site

ARS 136,828,000 - 197,640,000

Full time

7 days ago
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Job summary

IQVIA is seeking a Site Enablement Solutions Project Lead to optimize delivery across projects and act as a consultant to the study team. You will manage site identification, scope execution, and resource planning for global studies, coordinating with sponsors and internal teams to meet timelines and budget targets.

Role requires strong program management, 5 years of clinical trial experience, and fluent English for global collaboration.

Qualifications

  • Bachelor's degree in life sciences or related field.
  • 5 years' clinical trial experience.
  • 3 years' experience at a CRO or clinical trial services provider.
  • 3 years in a Project Manager role.
  • Advanced level of English, you'll work with global projects and global teams.

Responsibilities

  • Collaborate with pre- and post-award stakeholders to manage coordination, planning, and implementation of Site Enablement Solutions.
  • Develop global Site Enablement Solutions delivery strategy in identifying sites and extending services as warranted.
  • Determine internal team resourcing based on study needs.
  • Develop and execute operational plans for larger, multi-region studies and manage budgets.
  • Communicate with sponsors and project teams to monitor impact of Site Enablement Solutions.
  • Provide ongoing proactive operational and tactical recommendations based on study performance.
  • Establish study KPI and financial performance ownership and ensure quality deliverables.

Skills

Project management
English proficiency
CRO experience

Education

Bachelor's degree in life sciences or related field

Job description

IQVIA is seeking a Site Enablement Solutions Project Lead to optimize delivery across projects and act as a consultant to the study team. You will manage site identification, scope execution, and resource planning for global studies, coordinating with sponsors and internal teams to meet timelines and budget targets.

Role requires strong program management, 5 years of clinical trial experience, and fluent English for global collaboration.

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