Senior CRA — Lead Site Monitoring (60% Travel)

ICON Strategic Solutions; Lisboa; On-site; EUR 48,000 - 64,000; Full time

Benefits offered by this job

Health insurance

Annual leave

Retirement planning

Employee Assistance Program

Life insurance

Flexible benefits

Job summary

ICON Strategic Solutions in Lisbon is seeking aSenior Clinical Research Associate to oversee monitoring of clinical trials, ensuring adherence to protocol and GCP. The role comes within ICON's global sponsor-dedicated model and offers opportunities for professional growth.

You will lead on monitoring tasks requiring technical depth, collaborate with cross-functional teams, conduct site visits, ensure data integrity, and travel about 60% to sites across regions.

Qualifications

• Bachelor's degree in a scientific field required.
• Extensive CRA experience with regulatory knowledge.
• Ability to manage multiple sites and projects.

Responsibilities

• Lead clinical trial monitoring at assigned sites.
• Perform site visits and issue resolution for trial conduct.
• Collaborate with cross-functional teams for data collection and reporting.
• Provide training and guidance to site staff; travel ~60%.

Skills

Clinical trial monitoring

GCP compliance

Stakeholder management

Travel readiness

Education

Bachelor's degree in a relevant scientific discipline

Tools

CTMS

eTMF systems

Job description

ICON Strategic Solutions in Lisbon is seeking aSenior Clinical Research Associate to oversee monitoring of clinical trials, ensuring adherence to protocol and GCP. The role comes within ICON's global sponsor-dedicated model and offers opportunities for professional growth.

You will lead on monitoring tasks requiring technical depth, collaborate with cross-functional teams, conduct site visits, ensure data integrity, and travel about 60% to sites across regions.