Cancer Clinical Research Coordinator I (Hybrid Remote)

University of Wisconsin-Madison; Madison (WI); Hybrid; USD 50,000 - 61,000; Full time

Job summary

University of Wisconsin–Madison in Madison, WI is seeking a Clinical Research Coordinator I to support and coordinate cancer clinical trials across Disease-Oriented Teams. You will help ensure participants are safely enrolled, monitored, and supported, collaborating with clinical teams, research staff, and investigators as a key coordinator and point of contact.

The position focuses on ensuring study requirements are met, data and documentation are accurate, and participants are informed as they

Qualifications

• Experience with human subjects research preferred.
• Clinical research experience preferred.
• Experience working in a healthcare setting preferred.

Responsibilities

• Serves as an initial point of contact for clinical research participants and clinical staff, providing information regarding research procedures, expectations, and inquiries.
• Schedules logistics, determines workflows, and secures resources for a defined clinical research trial(s).
• Identifies work unit resources needs and manages supply and equipment inventory levels.
• Recruits, screens, selects, determines eligibility and enrolls trial participants, collects information, and answers questions under supervision of a medically licensed professional.
• Manages research workflow components, collects, prepares, processes, and submits participant data and samples to appropriate entities, adhering to research protocols.

Skills

Human subjects research

Clinical research

Education

Bachelor's degree preferred

Job description

University of Wisconsin–Madison in Madison, WI is seeking a Clinical Research Coordinator I to support and coordinate cancer clinical trials across Disease-Oriented Teams. You will help ensure participants are safely enrolled, monitored, and supported, collaborating with clinical teams, research staff, and investigators as a key coordinator and point of contact.

The position focuses on ensuring study requirements are met, data and documentation are accurate, and participants are informed as they