Clinical Trial Laboratory Network Lead

IQVIA

Buenos Aires

Presencial

ARS 1.200.000 - 2.000.000

Jornada completa

Hace 4 días
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Descripción de la vacante

IQVIA is seeking a capable laboratory project manager to oversee all lab activities for assigned clinical trial projects from startup through closeout. You will coordinate study setup, protocol and budget reviews, and lead meetings with customers.

The role requires strong interpersonal skills, experience in clinical research or lab environments, and solid knowledge of project management processes. You will work with multiple internal teams to ensure timely, compliant study delivery.

Formación

  • Bachelor's Degree Life Sciences or related field.
  • 2-3 years of experience in clinical trials/hospital-funded research, project management or laboratory environment preferred.
  • Strong interpersonal and customer management skills.
  • Working understanding of medical and clinical research terminology.
  • Working knowledge of Project Management processes and laboratory operations.

Responsabilidades

  • Manage all laboratory aspects of assigned clinical trial projects from startup to closeout.
  • Lead study setup planning, protocol reviews, and budget coordination; present materials at kickoff meetings.
  • Monitor timelines, budgets and study documentation; ensure quality and compliance.
  • Build and maintain customer relationships; serve as escalation point for study issues.

Educación

Bachelor's Degree Life Sciences
Equivalent combination of education, training and experience

Descripción del empleo

IQVIA is seeking a capable laboratory project manager to oversee all lab activities for assigned clinical trial projects from startup through closeout. You will coordinate study setup, protocol and budget reviews, and lead meetings with customers.

The role requires strong interpersonal skills, experience in clinical research or lab environments, and solid knowledge of project management processes. You will work with multiple internal teams to ensure timely, compliant study delivery.

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