Senior Clinical Research Associate

Job Summary

Managing research activities at clinical sites, the full-time Senior Clinical Research Associate will oversee all stages of clinical studies, including site identification, study initiation visits, and compliance monitoring, while working remotely.

Key responsibilities

• Manage research activities at participating clinical sites for various projects
• Conduct study initiation visits and ensure compliance with regulatory requirements
• Support site training on data collection and report safety-related events

Required qualifications

• 5+ years of experience as a Clinical Research Associate
• 4-year university degree or Nursing Degree
• Experience in Oncology is required
• Proficiency in Microsoft Office, CTMS, and EDC Systems
• Ability to work independently with minimal supervision