Oncology Clinical Research Associate

Responsibilities

• Conduct site and study visits and perform all site monitoring activities across multiple studies
• Responsible for both remote and on-site monitoring and study activation
• Participate in the development of study tools, protocols, and clinical trial documentation
• Some travel required once travel bands are lifted

Qualifications

• 3+ years of Oncology on-site Monitoring and hands-on experience with EDC Systems
• Experience with Phase 1 Oncology is non-negotiable
• Organization to perform monitoring duties across multiple sites is a must

Compensation

Salary Range: $110,000-$135,000
Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays