Clinical Trial Site Monitor II — Hybrid

ICON; Ciudad de México; Hybrid; MXN 600,000 - 800,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme (

Life assurance

Country-specific benefits

Job summary

ICON Strategic Solutions in Mexico City is seeking an SMA II to support management and monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and GCP guidelines. The role is office-based for the first four months, followed by a hybrid model.

You will coordinate site monitoring activities, assist with regulatory documents, collaborate with cross-functional teams, track site performance, and mentor junior staff in trial management.

Qualifications

• Bachelor's degree in life sciences, healthcare administration, or clinical research.
• Experience in clinical research, site management, or monitoring with knowledge of GCP.
• Strong organizational and project management skills with attention to deadlines.

Responsibilities

• Coordinate monitoring activities at clinical trial sites per study protocols.
• Assist in preparing and reviewing regulatory documents for regulatory compliance.
• Collaborate with cross-functional teams to support trial sites throughout the lifecycle.
• Track site performance metrics and generate reports for site management.
• Mentor junior staff to develop their clinical trial management skills.

Skills

Clinical research

Site management

Monitoring

Regulatory documents

Communication

Education

Bachelor's degree in life sciences/healthcare/clinical research

Job description

ICON Strategic Solutions in Mexico City is seeking an SMA II to support management and monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and GCP guidelines. The role is office-based for the first four months, followed by a hybrid model.

You will coordinate site monitoring activities, assist with regulatory documents, collaborate with cross-functional teams, track site performance, and mentor junior staff in trial management.