CTA/CSA (Payments)

Clinical Trial Associate position at ICON Strategic Solutions supporting sponsor-dedicated clinical research operations. The role involves coordinating trial administration, managing documentation, and ensuring regulatory compliance while working with cross-functional teams in a fast-paced research environment.

Responsibilities

• Coordinate and administer clinical trials while ensuring protocol compliance and regulatory adherence
• Maintain and organize clinical trial documentation, study files, and regulatory submissions
• Support preparation of study materials including informed consent and case report forms
• Facilitate cross-functional team communication to ensure smooth trial execution
• Track and report clinical trial metrics and milestones

Requirements

• Bachelor's degree in 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 with attention to detail
• Willingness to travel approximately 10% as required