Certified Clinical Research Specialist

Job Summary

Overseeing the clinical trial activation process, the full-time Certified Clinical Research Specialist will act as a liaison between central departments and research teams, ensuring all institutional requirements are met prior to activation while maintaining real-time tracking of trial progress and milestones in a remote work environment.

Key responsibilities

• Facilitate protocol acceptance, activation, and modification implementation for clinical research studies
• Maintain up-to-date status updates and serve as a primary resource for study status information across assigned trials
• Ensure appropriate regulatory documentation and standard operating procedures are maintained throughout the study lifecycle

Required qualifications

• Bachelor's Degree required; Master's Degree preferred
• Four years of experience in regulatory compliance or clinical research start-up
• Certification as a Clinical Research Professional (CCRP), Clinical Research Coordinator (CCRC), or Clinical Research Associate (CCRA) required
• Knowledge of institutional policies and clinical trial workflows
• Ability to develop and maintain tracking systems for protocol activations and modifications