Remote LATAM Centralized Monitoring Lead

Avos Tech | Chile; Cerrillos; A distancia; CLP 87.634.000 - 126.582.000; Jornada completa

Descripción de la vacante

IQVIA seeks a Centralized Monitoring Lead for LATAM to drive oversight of clinical deliverables across global projects on a remote basis. You will partner with project and clinical leads to optimize speed, quality and cost, while adhering to IQVIA SOPs and regulatory requirements.

The role requires leadership, strong communication, and a track record in clinical monitoring, with experience across multi-country studies and RBM analytics.

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 command of 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

• Leadership activities: Lead Centralized Monitoring team and oversee clinical deliverables per protocol, SOPs and regulations.
• Unblinded Clinical Lead responsibilities including IP management and risk mitigation.
• Manage project resources (CRAs/ Central Monitors/ Clinical Trial Assistants/ Centralized Monitoring Assistants).
• Monitor study/site metrics and trend analysis; develop analytics strategy and RBM tools.
• Support monitoring strategy development and study team/ client meetings.
• Ensure documentation and eTMF readiness; promote continuous process improvements.

Descripción del empleo

IQVIA seeks a Centralized Monitoring Lead for LATAM to drive oversight of clinical deliverables across global projects on a remote basis. You will partner with project and clinical leads to optimize speed, quality and cost, while adhering to IQVIA SOPs and regulatory requirements.

The role requires leadership, strong communication, and a track record in clinical monitoring, with experience across multi-country studies and RBM analytics.