Clinical Trial Associate
ICON · Prague, Czechia
Clinical OperationsFull-timeCompany career page
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Role summary
Clinical Trial Associate position supporting the design, coordination, and administration of clinical trials. The role involves managing trial documentation, ensuring regulatory compliance, and collaborating with cross-functional teams. Requires a bachelor's degree in a scientific or healthcare field, minimum one year of clinical research experience, and fluency in Czech and English.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 1 year experience as Clinical Trial Associate or similar role
- Fluency in Czech and English languages
- Knowledge of clinical trial processes, regulations, and guidelines
- Strong organizational and communication skills
- Ability to work collaboratively in fast-paced environment with attention to detail
- Willingness to travel approximately 10% as required
What you'll be doing
- Assist in coordination and administration of clinical trials while ensuring protocol and regulatory compliance
- Maintain and organize clinical trial documentation including study files and regulatory submissions
- Support preparation of study-related materials such as informed consent and case report forms
- Work with cross-functional teams to facilitate communication and ensure trial execution
- Track and report clinical trial metrics and milestones
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.