Senior CRA – Global Monitoring Lead

ICON San Antonio; Paris; Presencial; EUR 70.000 - 90.000; Jornada completa

Descripción de la vacante

ICON Plc, a sponsor-focused global CRO, is seeking a Senior Clinical Research Associate in Paris to oversee monitoring activities in a sponsor-dedicated model. You will ensure trials comply with protocol, GCP, and regulatory standards while working closely with cross-functional teams.

You will travel ~60% and lead on-site monitoring, provide training, and build relationships with site staff to drive successful trial execution and data quality.

Formación

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience as a Clinical Research Associate with strong regulatory knowledge.
• 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 skills to drive compliance.
• Willingness to travel approximately 60%.

Responsabilidades

• Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conduct site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Conocimientos

Clinical trial monitoring

Regulatory compliance

Data integrity

Stakeholder management

Travel readiness

Educación

Bachelor's degree

Herramientas

Clinical trial software

Descripción del empleo

ICON Plc, a sponsor-focused global CRO, is seeking a Senior Clinical Research Associate in Paris to oversee monitoring activities in a sponsor-dedicated model. You will ensure trials comply with protocol, GCP, and regulatory standards while working closely with cross-functional teams.

You will travel ~60% and lead on-site monitoring, provide training, and build relationships with site staff to drive successful trial execution and data quality.