Protocol Activation Coordinator

Job Summary

To support the activation and management of research studies, the full-time remote Protocol Activation Coordinator will manage project workflows, assist with regulatory documentation, and collaborate with various stakeholders to ensure compliance and operational efficiency.

Key responsibilities

• Manages processing, tracking, and filing of study documents and updates
• Collaborates with Investigators and study teams to gather and maintain essential regulatory documents
• Assists Project Managers in study oversight responsibilities and supports study management activities

Required qualifications

• Bachelor's degree in a related field and two years of relevant experience or equivalent combination of education and experience
• Demonstrated understanding of regulatory compliance related to clinical research
• Experience with clinical trial processes, HIPAA regulations, and IRB requirements
• Proficiency in using technological systems related to clinical research and data management
• Strong organizational skills with the ability to manage multiple projects and shifting priorities