Oncology Sr. CRA I

Job Summary

A company is looking for a Senior Clinical Research Associate I on the West Coast with oncology experience.

Key Responsibilities

• Monitor study sites, including routine monitoring, close-out, and maintenance of study files
• Ensure compliance with informed consent procedures and protocol requirements to protect study patients
• Assist with training of new employees and coordinate designated clinical projects as a Local Project Coordinator

Required Qualifications

• University or college degree, or certification in a related allied health profession
• 3+ years of clinical monitoring experience
• Oncology experience is required
• Open to major hub locations on the West Coast (CA, NV, AZ, ID, NM, OR, WA)