Clinical Trial Associate: Global Collaboration in Trials

ICON Clinical Research; Utrecht; On-site; EUR 40,000 - 60,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning options

Global Employee Assistance Programme (

Life assurance

Job summary

ICON Strategic Solutions is seeking a Clinical Trial Associate in Utrecht. You will assist with design and analysis of clinical trials, interpret complex medical data, and contribute to advancing treatments.

Your responsibilities include coordinating trials, maintaining documents, preparing materials, and working with cross-functional teams to ensure smooth execution and timely metrics reporting.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Prior experience or strong interest in clinical research.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.
• Ability to work collaboratively in a fast-paced environment with attention to detail.
• Willingness to travel approximately 10%

Responsibilities

• Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
• Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
• Support the preparation of study-related materials, such as informed consent forms and case report forms.
• Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
• Contribute to the tracking and reporting of clinical trial metrics and milestones.

Skills

Communication skills

Organization

Team collaboration

Attention to detail

Travel readiness

Education

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

Job description

ICON Strategic Solutions is seeking a Clinical Trial Associate in Utrecht. You will assist with design and analysis of clinical trials, interpret complex medical data, and contribute to advancing treatments.

Your responsibilities include coordinating trials, maintaining documents, preparing materials, and working with cross-functional teams to ensure smooth execution and timely metrics reporting.