Clinical Trial Associate: Drive Trial Coordination & Data

ICON Strategic Solutions; Utrecht; On-site; EUR 42,000 - 62,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Global EAP LifeWorks program

Life assurance

Country-specific benefits

Job summary

ICON Strategic Solutions is seeking a Clinical Trial Associate to help design and analyze clinical trials and interpret medical data, contributing to the development of innovative treatments. You will work with a dedicated team to coordinate trials, maintain documentation, and ensure regulatory compliance while benefiting from global support and career growth.

Fluency in Dutch and English and a relevant degree are required.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Experience or strong interest in clinical research.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.
• Fluent in Dutch and English.

Responsibilities

• Assist in coordination and administration of clinical trials, ensuring regulatory compliance.
• Maintain and organize trial documentation and regulatory submissions.
• Support preparation of informed consent forms and case report forms.
• Collaborate with cross-functional teams to ensure smooth trial execution.
• Track and report clinical trial metrics and milestones.

Skills

Dutch

English

Education

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

Job description

ICON Strategic Solutions is seeking a Clinical Trial Associate to help design and analyze clinical trials and interpret medical data, contributing to the development of innovative treatments. You will work with a dedicated team to coordinate trials, maintain documentation, and ensure regulatory compliance while benefiting from global support and career growth.

Fluency in Dutch and English and a relevant degree are required.