Senior Clinical Research Associate – Site Monitoring Lead

KCR Placement; Lisboa; On-site; EUR 45,000 - 65,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning

Global Employee Assistance Programme (

Life assurance

Country-specific optional benefits

Job summary

ICON Strategic Solutions is seeking a Senior Clinical Research Associate to join ICON Plc. You will oversee and manage clinical trial activities to ensure studies run to protocol, regulatory requirements and GCP standards.

This role emphasizes hands-on monitoring with a focus on quality and continuous improvement. You will lead on monitoring tasks, visit sites, support data collection and reporting, train site staff and build strong relationships with site personnel to enable smooth trial

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience as a Clinical Research Associate with strong regulatory knowledge.
• Proven ability to manage multiple sites and projects simultaneously.
• Expertise in monitoring practices and data integrity.
• Excellent communication and stakeholder management skills.

Responsibilities

• Monitor clinical trial sites to ensure adherence to protocols and GCP.
• Conduct site visits to assess performance and resolve issues.
• Collaborate with crossfunctional teams to ensure timely data collection and reporting.
• Provide training and guidance to site staff and other CRAs.
• Build and maintain relationships with site personnel and stakeholders.

Skills

Monitoring practices

Data integrity

Site management

Communication skills

Stakeholder management

Travel readiness

Education

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

Job description

ICON Strategic Solutions is seeking a Senior Clinical Research Associate to join ICON Plc. You will oversee and manage clinical trial activities to ensure studies run to protocol, regulatory requirements and GCP standards.

This role emphasizes hands-on monitoring with a focus on quality and continuous improvement. You will lead on monitoring tasks, visit sites, support data collection and reporting, train site staff and build strong relationships with site personnel to enable smooth trial