Senior CRA - Oncology Trials Lead (Mexico, 60% Travel)

ICON; México; On-site; MXN 600,000 - 900,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Employee Assistance Programme (LifeW o

Life assurance

Country-specific benefits

Job summary

ICON Plc in Mexico City is seeking a Senior Clinical Research Associate to oversee monitoring activities, ensuring protocol adherence and regulatory compliance. The role follows a sponsor-dedicated model, leveraging ICON’s global expertise to support trial execution.

You will lead on monitoring tasks with a focus on quality, collaborate with cross-functional teams, and travel ~60% to sites to ensure timely, accurate data collection and robust study progress.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience as a Clinical Research Associate with regulatory knowledge.
• Proven ability to manage multiple sites and projects with strong organizational skills.
• Expertise in monitoring practices, data integrity, and site management with trial software proficiency.
• Excellent communication and stakeholder management skills; ability to drive compliance.
• Willingness to travel approximately 60%.

Responsibilities

• Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP standards.
• Conduct site visits to assess site performance, resolve issues, and support trial execution.
• Collaborate with cross-functional teams for timely data collection and reporting.
• Provide training and guidance to site staff to maintain high trial conduct standards.
• Build and maintain relationships with site personnel and stakeholders to facilitate operations.

Skills

Clinical trial monitoring

Regulatory knowledge

Data integrity

Site management

Stakeholder management

Travel readiness

Education

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Tools

Clinical trial software

Data management tools

Job description

ICON Plc in Mexico City is seeking a Senior Clinical Research Associate to oversee monitoring activities, ensuring protocol adherence and regulatory compliance. The role follows a sponsor-dedicated model, leveraging ICON’s global expertise to support trial execution.

You will lead on monitoring tasks with a focus on quality, collaborate with cross-functional teams, and travel ~60% to sites to ensure timely, accurate data collection and robust study progress.