Clinical Trial Associate

Job Summary

Clinical Trial Associate coordinates activities on clinical research trials in a full-time remote position, working with clinical teams to manage trial-related tasks and documentation.

Key Responsibilities

• Update and maintain clinical systems and documentation within timelines
• Draft trial plans, create trial documents, and serve as a central contact for trial communications
• Gather and maintain essential regulatory documents and prepare trial materials for investigative sites

Required Qualifications

• Associate's degree in a life science or health-related field preferred; experience may substitute for education
• Minimum of 2 years of experience in an administrative role
• Minimum of 2 years of experience in support of clinical research, preferably in oncology
• Proficiency with Microsoft Office applications
• Knowledge of GCP, ICH guidelines, and clinical trial regulations