Senior Clinical Trial Lead: Coordination & Quality

ICON Strategic Solutions; España; On-site; EUR 40,000 - 60,000; Full time

Benefits offered by this job

Health insurance

Retirement planning

Life assurance

Global EAP

Job summary

ICON Strategic Solutions is seeking a Senior Clinical Trial Assistant to oversee and support the execution of clinical trials, ensuring quality, compliance and efficiency. You will work in a sponsor-dedicated model, supported by ICON’s global expertise.

You will lead clinical coordination tasks, manage trial activities to protocols and timelines, oversee site management and data integrity, and mentor staff while collaborating with cross-functional teams across studies.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare field.
• Significant experience in clinical trial management.
• Ability to manage multiple projects with strong organization.
• Excellent communication and collaboration with diverse teams.
• Detail-oriented with proactive problem-solving.

Responsibilities

• Lead clinical coordination tasks focusing on quality and continuous improvement.
• Manage and coordinate clinical trial activities to meet protocols and timelines.
• Collaborate with cross-functional teams to address trial issues and optimize processes.
• Oversee site management and monitoring to ensure data integrity.
• Provide guidance to clinical staff and investigators on best practices and regulatory standards.
• Track trial progress and identify risks with mitigation strategies.

Skills

Clinical coordination

Project management

Regulatory compliance

Communication skills

Detail oriented

Education

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

Job description

ICON Strategic Solutions is seeking a Senior Clinical Trial Assistant to oversee and support the execution of clinical trials, ensuring quality, compliance and efficiency. You will work in a sponsor-dedicated model, supported by ICON’s global expertise.

You will lead clinical coordination tasks, manage trial activities to protocols and timelines, oversee site management and data integrity, and mentor staff while collaborating with cross-functional teams across studies.