Remote Centralized Monitoring Lead (LATAM)

Maxit Consulting - Max Corporate Group; La Pampa; A distancia; ARS 136.687.000 - 197.436.000; Jornada completa

Descripción de la vacante

IQVIA in LATAM is seeking a Centralized Monitoring Lead for remote work across Argentina, Brazil, Peru, Colombia, and more. You will oversee clinical deliverables, manage a global monitoring team, and drive RBM strategies to ensure compliance and data integrity.

The role requires a lead experience, strong English, and deep knowledge of ICH GCP and regulatory guidelines. Collaboration with project teams and continuous process improvements are essential.

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 including advanced English.
• Strong organizational, problem solving and decision making skills.
• Results and detail-oriented approach to work delivery.
• Excellent motivational, influencing, negotiating and coaching skills.

Responsabilidades

• Lead the Centralized Monitoring team and oversee clinical deliverables on global projects as per protocol and SOPs.
• Act as Unblinded Clinical Lead and manage IP, risk, and mitigations for assigned studies.
• May act as Clinical Lead when not assigned to a study and at project close out.
• Manage project resources (CRAs, Central Monitors, Clinical Trial Assistants).
• Develop monitoring strategy and RBM tools; monitor study metrics and trends.
• Attend study team or client meetings and provide inputs for process improvements.
• Ensure documentation and audit readiness (eTMF oversight).
• Mentor junior staff.

Descripción del empleo

IQVIA in LATAM is seeking a Centralized Monitoring Lead for remote work across Argentina, Brazil, Peru, Colombia, and more. You will oversee clinical deliverables, manage a global monitoring team, and drive RBM strategies to ensure compliance and data integrity.

The role requires a lead experience, strong English, and deep knowledge of ICH GCP and regulatory guidelines. Collaboration with project teams and continuous process improvements are essential.