Remote LATAM Centralized Monitoring Lead

Clubshop | Us; Gualeguaychú; A distancia; ARS 137.157.000 - 228.596.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Centralized Monitoring Lead for LATAM. This remote role collaborates with project and clinical leads to deliver study objectives while optimizing speed, quality, and cost.

You will oversee global deliverables, manage a team of CRAs and monitors, and ensure regulatory compliance and data integrity across studies. The position requires a strong background in clinical monitoring, leadership experience, and excellent English communication.

Formación

• Bachelor's degree in life sciences or related field.
• +3 years of relevant clinical monitoring experience (remote or on-site CRA).
• +2 years in a Lead role.
• Strong written and verbal communication skills including English (Mandatory).
• Strong organizational, problem solving and decision making skills.
• Results- and detail-oriented approach to work delivery and output.
• Excellent motivational, influencing, negotiating and coaching skills.
• Ability to work on multiple global projects and manage competing priorities.
• To lead team and effectively work in team.

Responsabilidades

• Provide oversight on clinical deliverables for global projects according to protocols and SOPs.
• Act as Unblinded Clinical Lead and manage IP, supply and labeling issues.
• Lead the Centralized Monitoring team and manage resources.
• Monitor study/site metrics and coordinate action plans.
• Develop analytics strategy and RBM tools.
• Support monitoring strategy development and client meetings.
• Ensure documentation and eTMF readiness.
• Mentor junior staff.

Conocimientos

Leadership

English proficiency

Clinical monitoring

Team management

Communication

Problem solving

Educación

Bachelor's degree in life sciences

Descripción del empleo

IQVIA is seeking a Centralized Monitoring Lead for LATAM. This remote role collaborates with project and clinical leads to deliver study objectives while optimizing speed, quality, and cost.

You will oversee global deliverables, manage a team of CRAs and monitors, and ensure regulatory compliance and data integrity across studies. The position requires a strong background in clinical monitoring, leadership experience, and excellent English communication.