Senior Clinical Trial Coordination Lead

ICON Clinical Research; España; A distancia; EUR 28.000 - 42.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual leave entitlements

Health insurance

Competitive retirement planning

Global Employee Assistance Programme (

Life assurance

Flexible country-specific benefits

Descripción de la vacante

ICON Strategic Solutions is seeking a Clinical Trial Assistant to join a sponsor‑dedicated model backed by ICON’s global expertise. You will oversee and support trial execution with a strong focus on quality and compliance.

You will coordinate clinical activities, manage site work, collaborate with cross‑functional teams, and help monitor timelines, data integrity, and regulatory adherence to ensure successful study outcomes.

Formación

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Significant experience in clinical trial management and regulatory requirements.
• Ability to manage multiple projects with strong organization and problem‑solving.
• Excellent communication and interpersonal skills with diverse stakeholders.
• Detail‑oriented with proactive approach to trial success.

Responsabilidades

• Managing and coordinating clinical trial activities to ensure adherence to protocols and timelines.
• Collaborating with cross-functional teams to address trial issues and optimize processes.
• Overseeing site management and monitoring for data integrity and regulatory compliance.
• Providing guidance to clinical staff and investigators on best practices and standards.
• Tracking and reporting trial progress, identifying risks, and mitigating challenges.

Conocimientos

Clinical coordination

Clinical trial management

Organizational skills

Problem solving

Communication skills

Educación

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

Descripción del empleo

ICON Strategic Solutions is seeking a Clinical Trial Assistant to join a sponsor‑dedicated model backed by ICON’s global expertise. You will oversee and support trial execution with a strong focus on quality and compliance.

You will coordinate clinical activities, manage site work, collaborate with cross‑functional teams, and help monitor timelines, data integrity, and regulatory adherence to ensure successful study outcomes.