Clinical Site Monitor I - Flexible Mexico Office

ICON Strategic Solutions; México; Hybrid; MXN 250,000 - 360,000; Full time

Benefits offered by this job

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme (

Life assurance

Flexible country-specific benefits

Job summary

ICON Strategic Solutions in Mexico City offers a sponsor‑dedicated environment where you contribute to clinical trial sites under ICON’s global expertise. As a SMA I, you will assist with site monitoring, ensure protocol compliance, and support efficient site operations.

You will work with cross‑functional teams, maintain records, and participate in ongoing training to grow in clinical trial management. Some travel is required.

Qualifications

• Bachelor's degree in a life sciences, healthcare or clinical research field.
• Some experience in clinical research, site management, or related admin roles is preferred.
• Strong organizational skills and attention to detail for multitasking.
• Basic knowledge of clinical trial processes and regulatory requirements is a plus.
• Excellent communication and teamwork abilities; willing to travel ~25%.

Responsibilities

• Assist in monitoring clinical trial sites and ensure protocol compliance.
• Support site management activities, including documentation and data entry.
• Collaborate with cross‑functional teams to address site‑related issues.
• Maintain accurate site activity records and contribute to monitoring reports.
• Participate in training to enhance site management knowledge.

Skills

Clinical research

Site management

Organizational skills

Communication skills

Travel readiness

Education

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

Tools

GCP knowledge

Data entry systems

Job description

ICON Strategic Solutions in Mexico City offers a sponsor‑dedicated environment where you contribute to clinical trial sites under ICON’s global expertise. As a SMA I, you will assist with site monitoring, ensure protocol compliance, and support efficient site operations.

You will work with cross‑functional teams, maintain records, and participate in ongoing training to grow in clinical trial management. Some travel is required.