Clinical Research Associate

Job Summary

Supporting key clinical trial activities in a full-time remote capacity, the Internal Clinical Research Associate will manage site activation, maintain essential study documents, and collaborate with clinical study teams to ensure compliance with regulatory requirements and quality standards.

Key responsibilities

• Support site identification, qualification, activation, monitoring, and closeout activities across clinical studies
• Maintain Trial Master Files and essential study documents to ensure inspection readiness and regulatory compliance
• Generate study newsletters and communications to support investigator sites and cross-functional stakeholders

Required qualifications

• Bachelor's degree in Life Sciences or a related scientific discipline
• 0+ years of experience in clinical research or related fields