Central Monitor II – Remote (Mexico)

About the role

The Central Monitor II will remotely review patient data for Phase I‑IV clinical research and non‑interventional studies. The role ensures protocol compliance, patient safety, and data integrity using analytical dashboards and reports.

Key responsibilities

• Review protocol, critical data, safety and data‑integrity risks related to study execution.
• Analyze patient data listings and visualizations to confirm eligibility, detect protocol deviations, safety concerns, and data anomalies.
• Assess factors affecting subject safety and data quality at investigator sites, including pharmacovigilance issues.
• Escalate serious issues promptly, develop action plans with guidance, and document observations.
• Generate queries, protocol deviation reports, and action items based on review findings.

Required profile

• Experience in clinical monitoring or data review for drug development studies.
• Strong understanding of ICH‑GCP, local and federal regulatory requirements.
• Ability to work independently, make sound judgments, and communicate findings clearly.
• Proficiency with analytical dashboards and data visualization tools.

Required skills

• Clinical monitoring
• ICH‑GCP knowledge
• Data review using analytical dashboards
• Pharmacovigilance awareness
• Protocol compliance assessment
• Documentation and query generation

What we offer

• Career development and progression opportunities.
• Supportive line management and technical/therapeutic training.
• Peer recognition and total rewards program.
• Inclusive culture that values authenticity.