Clinical Trial Associate
ICON
Clinical Trial Associate role supporting the design, coordination, and administration of clinical trials in a hybrid setting. The position involves managing trial documentation, regulatory compliance, and cross-functional collaboration to advance innovative treatments.
Responsibilities
- Coordinate and administer clinical trials while ensuring protocol and regulatory compliance
- Maintain and organize clinical trial documentation, study files, and regulatory submissions
- Support preparation of study materials including informed consent and case report forms
- Facilitate communication between cross-functional teams for smooth trial execution
- Track and report clinical trial metrics and milestones
Requirements
- Bachelor's degree in scientific or healthcare-related field
- Prior experience or demonstrated interest in clinical research
- Knowledge of clinical trial processes, regulations, and guidelines
- Strong organizational and communication skills
- Ability to work collaboratively with attention to detail
- Willingness to travel approximately 10% as required
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