Remote Centralized Monitoring Lead - LATAM

Serdan Sa; Valle del Cauca; A distancia; COP 280.260.000 - 404.820.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Remote work

Descripción de la vacante

IQVIA is seeking a Centralized Monitoring Lead to supervise a global team across LATAM and remote environments. You will partner with project and clinical leads to ensure delivery objectives are met with high quality and efficiency.

The role requires 3+ years in clinical monitoring, 2+ years in a lead position, and strong English communication. You will mentor staff and drive continuous process improvements while maintaining regulatory compliance.

Formación

• Bachelor’s degree in life sciences or related field.
• +3 years of relevant clinical monitoring experience (remote or on-site).
• +2 years in a Lead role.
• Strong written and verbal communication skills including advanced English (Mandatory).
• Strong organizational, problem solving and decision making skills.
• Ability to lead and work effectively in a team.

Responsabilidades

• Lead the Centralized Monitoring team across global projects, ensuring delivery per protocol and sponsor expectations.
• Oversee oversight of clinical deliverables, including risk identification and mitigation.
• Manage project resources (CRAs, Central Monitors, CTAs, Centralized Monitoring Assistants).
• Develop and implement study analytics strategies and monitoring plans.
• Attend study team and client meetings and communicate with key decision makers.
• Maintain complete documentation and drive audit readiness for eTMF and tools.
• Mentor and coach junior staff.

Conocimientos

Leadership

Communication

Organizational skills

Problem solving

Decision making

Team leadership

Educación

Bachelor's degree in life sciences or related field

Descripción del empleo

IQVIA is seeking a Centralized Monitoring Lead to supervise a global team across LATAM and remote environments. You will partner with project and clinical leads to ensure delivery objectives are met with high quality and efficiency.

The role requires 3+ years in clinical monitoring, 2+ years in a lead position, and strong English communication. You will mentor staff and drive continuous process improvements while maintaining regulatory compliance.