Clinical Trial Associate
HybridWarsaw, Mazovia, Poland
Job Summary
Coordinate and administer clinical trials while ensuring compliance with protocols and regulatory requirements. Maintain and organize clinical trial documentation, including study files and regulatory submissions, and support the preparation of materials such as informed consent forms and case report forms. Facilitate communication with cross-functional teams to ensure smooth trial execution and contribute to tracking and reporting clinical trial metrics and milestones. Requires a Bachelor's degree in a scientific or healthcare-related field, prior clinical research experience, and willingness to travel approximately 10%. This role supports ICON's mission to bring new medicines and treatments to patients faster through rigorous clinical research operations.
Required 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 as required (approximately 10%)
- Employment with ICON is contingent upon having the legal right to work in the country where the role is based
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.