Senior CRA – Oncology Trials | 60% Travel

ICON Clinical Research; México; Remote; MXN 700,000 - 900,000; Full time

Benefits offered by this job

Health insurance

Retirement planning

LifeWorks program

Life insurance

Childcare vouchers

Gym discounts

Job summary

ICON Plc, a world-leading FSP, offers a sponsor-dedicated model with global expertise and a focus on delivering quality trial work. The Senior CRA role involves monitoring, site visits, data integrity, and collaboration across teams to ensure compliant, timely trial execution.

The position requires 60% travel and a strong background in clinical trial monitoring, with the ability to guide and train others in a complex regulatory environment.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience as a Clinical Research Associate with understanding of trial processes and regulations.
• Ability to manage multiple sites and projects with strong organization and problem-solving skills.
• Expertise in monitoring practices, data integrity, and site management with relevant tools.
• Excellent communication and stakeholder management to drive compliance in a complex environment.
• Willingness to travel approximately 60%.

Responsibilities

• Lead clinical trial monitoring tasks with a focus on quality and continuous improvement.
• Conduct site visits to assess performance, resolve issues, and support trial execution.
• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
• Provide training and guidance to site staff and other CRAs to maintain high standards.
• Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth operations.

Skills

Clinical trial monitoring

Site management

Data integrity

Regulatory compliance

Problem-solving

Travel readiness

Education

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

Tools

Clinical trial software

Job description

ICON Plc, a world-leading FSP, offers a sponsor-dedicated model with global expertise and a focus on delivering quality trial work. The Senior CRA role involves monitoring, site visits, data integrity, and collaboration across teams to ensure compliant, timely trial execution.

The position requires 60% travel and a strong background in clinical trial monitoring, with the ability to guide and train others in a complex regulatory environment.