💼 About This Role

You'll serve as the trusted face to clinical practice at a site in Los Gatos, CA, supporting oncology clinical trials and ensuring data quality. You'll help bring better therapies to patients faster in a dynamic startup environment.

🎯 What You'll Do

• Obtain informed consent for clinical trials.
• Perform peer review of clinical documentation for data quality.
• Assist in patient recruitment strategies.
• Ensure adherence to study protocols and data completeness.

📋 Requirements

• 3+ years of experience in oncology clinical research.
• Bachelor's degree in health science or related field.
• Certified Clinical Research Coordinator (CCRC, CCRA, or CCRP).
• Knowledge of clinical trials and patient consent forms.

🚩 Heads Up

• Requires daily travel between sites but listed as on-site in one location.
• Mixes coordinator and DHS II responsibilities.