Remote Clinical Trial Associate — Mexico

ICON Strategic Solutions; México; Remote; MXN 360,000 - 540,000; Full time

Benefits offered by this job

Health insurance

Retirement planning

Global Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Job summary

ICON Strategic Solutions is seeking a Clinical Trial Associate for a home-based role in Mexico. You will support design and analysis of clinical trials, interpret complex medical data, and contribute to advancing treatments that benefit patients worldwide.

Your responsibilities include coordinating trials, organizing study files, preparing essential documents, and working with cross-functional teams to ensure timely execution and accurate reporting of trial metrics.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field is required.
• Strong organizational and communication skills are essential.
• Experience or interest in clinical research is preferred.
• Knowledge of clinical trial processes, regulations, and guidelines is desirable.
• Ability to work collaboratively in a fast-paced environment with attention to detail.

Responsibilities

• Assist in coordination and administration of clinical trials, ensuring protocol compliance.
• Maintain and organize study documentation and regulatory submissions.
• Support preparation of informed consent forms and case report forms.
• Coordinate with cross-functional teams to enable smooth trial execution.
• Help track and report clinical trial metrics and milestones.

Education

Bachelor's degree in science/healthcare

Job description

ICON Strategic Solutions is seeking a Clinical Trial Associate for a home-based role in Mexico. You will support design and analysis of clinical trials, interpret complex medical data, and contribute to advancing treatments that benefit patients worldwide.

Your responsibilities include coordinating trials, organizing study files, preparing essential documents, and working with cross-functional teams to ensure timely execution and accurate reporting of trial metrics.