Clinical Research Coordinator I

Role Overview

• Support and coordinate cancer clinical trials across Disease-Oriented Teams.
• Ensure participants are safely enrolled, monitored, and supported throughout research participation.
• Collaborate with clinical teams, research staff, and investigators.
• Contribute to the development of protocols and clinical research documents.
• Schedule logistics, determine workflows, and secure resources for trials.
• Recruit, screen, select, determine eligibility, and enroll trial participants.
• Perform medical assessments and quality checks.
• Serve as a main point of contact for clinical research participants.

Requirements

• At least 1 year of clinical research experience strongly preferred.
• Prior experience working in a healthcare setting preferred.
• Prior experience in oncology preferred.
• Bachelor's Degree preferred.

Benefits

• Health insurance
• Paid time off
• Professional development opportunities