FSP - Central Monitor in Mexico

Location: Home-based role in Mexico City, Mexico

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Perform centralized monitoring activities across assigned global clinical studies, typically supporting 4–5 studies simultaneously.
• Review site-level and study-level risk signals generated through centralized monitoring platforms.
• Analyze clinical and operational data to identify trends, anomalies, risks, and potential quality issues.
• Complete signal reviews within established timelines, typically within five business days of generation.
• Document findings and risk assessments, recommend mitigation actions, and track follow-up through resolution.
• Prepare reports, metrics, dashboards, and presentations while collaborating with CRAs, Risk Advisors, and cross-functional study teams.

Requirements

• Bachelor’s degree in Life Sciences.
• Previous experience in centralized monitoring review, clinical data review, risk-based monitoring, clinical data analytics, or central monitoring findings review.
• Advanced English proficiency is mandatory; the CV must be submitted in English.
• Strong written, verbal, and presentation skills.
• Proficiency with Microsoft Excel, reporting tools, and data visualization platforms.

Culture & Benefits

• Home-based work arrangement.
• Collaboration with global study teams and sponsor-designated Risk Advisors.
• Work focused on clinical data quality, patient safety, and risk-based study oversight.
• Opportunities to support continuous improvement of centralized monitoring and risk management processes.