Clinical Trial Site Monitor II – Office to Hybrid

ICON Clinical Research; Ciudad de México; On-site; MXN 400,000 - 700,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings for you and

Life assurance

Retirement planning offerings

Employee Assistance Programme

Flexible country-specific benefits

Job summary

ICON Clinical Research, based in Mexico City, seeks an SMA II to support management and monitoring of clinical trial sites in a sponsor-dedicated model, ensuring study protocols and GCP compliance. You will coordinate site monitoring, assist with regulatory documents, and collaborate across teams to optimize trial operations.

The role starts office-based for four months, then transitions to a hybrid model with ICON’s global teams, offering growth in a supportive, patient-focused environment.

Qualifications

• Experience in clinical research, site management, or monitoring.
• Solid understanding of clinical trial processes and GCP guidelines.
• Strong ability to manage multiple priorities and deadlines.
• Attention to detail and high-quality standards.

Responsibilities

• Coordinate monitoring activities at clinical trial sites and ensure protocol adherence.
• Assist in preparation and review of regulatory documents for site activities.
• Collaborate with cross-functional teams to support trial sites through the study lifecycle.
• Track site performance metrics and provide reports to improve site management.
• Mentor junior staff and support development in clinical trial management.

Skills

Organizational skills

Analytical skills

Communication skills

Interpersonal skills

Education

Bachelor's degree (life sciences, healthcare administration, or clinical research)

Job description

ICON Clinical Research, based in Mexico City, seeks an SMA II to support management and monitoring of clinical trial sites in a sponsor-dedicated model, ensuring study protocols and GCP compliance. You will coordinate site monitoring, assist with regulatory documents, and collaborate across teams to optimize trial operations.

The role starts office-based for four months, then transitions to a hybrid model with ICON’s global teams, offering growth in a supportive, patient-focused environment.