Remote Centralized Monitoring Lead (LATAM)

Maxit Consulting - Max Corporate Group

La Pampa

A distancia

ARS 137.157.000 - 198.116.000

Jornada completa

Hace 11 días
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Descripción de la vacante

IQVIA in LATAM seeks a Centralized Monitoring Lead to partner with project and clinical leads to deliver study objectives per contract, while optimizing speed, quality and cost, in line with IQVIA SOPs. Responsibilities include leading the Centralized Monitoring team, overseeing study deliverables, managing resources, and developing analytics strategy.

Strong English and regulatory knowledge required. This remote LATAM role requires 3+ years in clinical monitoring, 2+ years in lead roles, and

Formación

  • Bachelor's degree in life sciences or related field.
  • +3 years of clinical monitoring experience (remote or on-site CRA).
  • +2 years in a Lead role.
  • Advanced knowledge of ICH GCP and local regulations.
  • Excellent written and verbal English communication.
  • Ability to manage multiple global projects and priorities.

Responsabilidades

  • Lead the Centralized Monitoring team and oversee global study deliverables.
  • Manage resources (CRAs, Central Monitors, CTAs, Centralized Monitoring Assistants).
  • Develop study analytics strategy and advanced analytics.
  • Support monitoring strategy and triggers/thresholds.
  • Ensure audit-ready documentation and RBM tools.
  • Mentor junior staff.

Conocimientos

Team leadership
English proficiency
Clinical monitoring
Regulatory knowledge
Project management
Analytical skills

Educación

Bachelor's degree in life sciences

Descripción del empleo

IQVIA in LATAM seeks a Centralized Monitoring Lead to partner with project and clinical leads to deliver study objectives per contract, while optimizing speed, quality and cost, in line with IQVIA SOPs. Responsibilities include leading the Centralized Monitoring team, overseeing study deliverables, managing resources, and developing analytics strategy.

Strong English and regulatory knowledge required. This remote LATAM role requires 3+ years in clinical monitoring, 2+ years in lead roles, and

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