Director, Global Site Monitoring (Remote)

Ladders

United States

A distancia

USD 154.000 - 243.000

Jornada completa

hace 34 horas
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Ventajas ofrecidas por este puesto de trabajo

Comprehensive health and wellness
Flexible work arrangements
Professional development and training
Talent development and succession
Transparent compensation practices

Descripción de la vacante

Ladders, a leader in Pharmaceuticals & Biotech, seeks an Associate Director, Site Monitoring to guide a critical clinical operations function that supports high-quality study execution across global programs. The role focuses on site monitoring strategy, risk-based oversight, and compliant monitoring practices.

You will partner closely with cross-functional clinical teams to resolve site issues, maintain timelines and budgets, and strengthen trial execution.

Formación

  • Bachelor's degree in Life Sciences or equivalent; advanced degree preferred.
  • 8+ years in CRA or clinical site monitoring management in biotech, pharma, or CRO.
  • Experience with global teams and ICH/GCP standards.
  • Knowledge of risk-based monitoring models and clinical systems.

Responsabilidades

  • Lead site monitoring activities to ensure quality, timelines, and budget.
  • Drive execution of the site's monitoring strategy, including Risk-Based Monitoring.
  • Oversee compliance and quality of site monitoring planning and execution.
  • Serve as escalation point for site-related issues and ensure timely resolution.
  • Contribute to study phases through operational oversight of site monitoring.
  • Provide line management and development for Site Monitors and Leads.
  • Collaborate with cross-functional teams to ensure seamless study execution.

Conocimientos

Leadership
Global teams
Site monitoring
Risk-based monitoring
ICH/GCP knowledge
Budget management
Cross-functional collaboration
Problem solving

Educación

Bachelor's degree in Life Sciences or equivalent
Advanced degree preferred

Herramientas

CTMS
EDC
eTMF
eCOA

Descripción del empleo

Ladders, a leader in Pharmaceuticals & Biotech, seeks an Associate Director, Site Monitoring to guide a critical clinical operations function that supports high-quality study execution across global programs. The role focuses on site monitoring strategy, risk-based oversight, and compliant monitoring practices.

You will partner closely with cross-functional clinical teams to resolve site issues, maintain timelines and budgets, and strengthen trial execution.

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