California Licensed Clinical Research Associate

Job Summary

A company is looking for a Clinical Research Associate specializing in oncology with a focus on start-up processes.

Key Responsibilities

• Collaborate with teams to select and activate clinical trial sites in line with project timelines
• Perform Site Qualification Visits and maintain documentation for compliance and inspections
• Act as the main point of contact for sites and provide regular updates on project milestones

Required Qualifications and Education

• B.S., R.N., or equivalent degree, preferably in Biological Sciences
• 2-3 years of experience in monitoring pharmaceutical industry clinical trials
• 1-3 years of experience specifically in oncology clinical trials
• In-depth knowledge of Good Clinical Practice and ICH guidelines
• Legally authorized to work in the United States without requiring sponsorship