Certified Clinical Research Specialist

Job Summary

A company is looking for a Clinical Trial Activation Specialist who oversees the clinical trial activation process and acts as a liaison between departments and research teams.

Key Responsibilities

• Facilitate protocol acceptance, activation, and modification implementation for clinical research studies
• Maintain real-time tracking of study status and document delays in activation processes
• Ensure all institutional requirements are met prior to study activation and maintain regulatory documentation

Required Qualifications

• Required: Bachelor's Degree; preferred: Master's Degree
• Required: Four years of experience in regulatory compliance or clinical research start-up
• Required: CCRP, CCRC, or CCRA certification
• Experience may substitute education on a one-to-one basis
• Up-to-date knowledge of institutional policies and clinical trial workflows