Clinical Research Associate

Responsibilities

• Ensure compliance with standard protocol and regulatory and ICH GCP obligations in clinical site monitoring
• Complete on-site and remote monitoring activities including source document verification
• Write and submit reports of investigational site findings and update tracking systems
• Escalate observed deficiencies and issues as appropriate

Requirements

• Minimum Bachelor’s degree in a life science-related field or RN certification
• 3+ years of experience in clinical trials research
• Specific in vitro diagnostics study experience
• General knowledge of regulatory requirements and GCP
• High proficiency in Veeva Vault and Medrio
• Strong organizational and communication skills

Preferred Qualifications

• CRA certification by a recognized professional organization
• Previous experience in the cancer early detection space

About the Company

Freenome is dedicated to changing the landscape of cancer through advanced clinical development and diagnostics.