Senior CRA – Global Trial Monitoring, 60% Travel

KCR Placement; Paris; Híbrido; EUR 55.000 - 75.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual leave entitlements

Health insurance

Retirement planning

Global Employee Assistance Programme

Life assurance

Country-specific benefits

Descripción de la vacante

ICON Strategic Solutions is seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities, ensuring compliance with protocol, regulatory requirements, and industry standards.

You will lead monitoring tasks with a focus on quality and continuous improvement, visiting sites, resolving issues, and guiding staff while collaborating with cross-functional teams to ensure accurate data collection and reporting.

Formación

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

Responsabilidades

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

Conocimientos

Clinical trial monitoring

Site management

Data integrity

Cross-functional collaboration

Stakeholder management

Travel readiness

Educación

Bachelor's degree in life sciences

Descripción del empleo

ICON Strategic Solutions is seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities, ensuring compliance with protocol, regulatory requirements, and industry standards.

You will lead monitoring tasks with a focus on quality and continuous improvement, visiting sites, resolving issues, and guiding staff while collaborating with cross-functional teams to ensure accurate data collection and reporting.