Senior CRA – Oncology | Remote Spain | 60% Travel

ICON Clinical Research; Madrid; Remote; EUR 45,000 - 65,000; Full time

Benefits offered by this job

Annual leave

Health insurance offerings

Retirement planning

LifeWorks Employee Assistance Program

Flexible country-specific benefits

Job summary

ICON Plc is seeking a Senior Clinical Research Associate for a home-based role covering Madrid and Barcelona. You will oversee monitoring of clinical trials, ensuring adherence to protocol and GCP, while collaborating with cross-functional teams to maintain data quality and timely reporting.

Ideal candidates have oncology and Phase I exposure, proven CRA experience, and willingness to travel ~60%. The position emphasizes independence, scientific rigor, and leadership in trial execution.

Qualifications

• Bachelor’s degree in a relevant scientific field.
• Extensive CRA experience with strong regulatory knowledge.
• Ability to manage multiple sites and projects with organization.
• Proficiency in monitoring, data integrity and site management.
• Willingness to travel approximately 60%.

Responsibilities

• Lead clinical trial monitoring tasks with a focus on quality.
• Monitor sites for adherence to protocols and GCP requirements.
• Conduct site visits to assess performance and resolve issues.
• Collaborate with cross-functional teams for data collection and reporting.
• Provide training and guidance to site staff and other CRAs.

Skills

CRA experience

GCP/regulatory knowledge

Data integrity

Site management

Travel readiness

Oncology experience

Phase I experience

Education

Bachelor's degree in life sciences

Tools

Clinical trial software

EDC systems

Job description

ICON Plc is seeking a Senior Clinical Research Associate for a home-based role covering Madrid and Barcelona. You will oversee monitoring of clinical trials, ensuring adherence to protocol and GCP, while collaborating with cross-functional teams to maintain data quality and timely reporting.

Ideal candidates have oncology and Phase I exposure, proven CRA experience, and willingness to travel ~60%. The position emphasizes independence, scientific rigor, and leadership in trial execution.