Radiation Oncology Research Coordinator I

Washington University in St. Louis; Forest Park (OH); On-site; USD 49,000 - 74,000; Full time

Benefits offered by this job

Health insurance

Metro transit U-Pass

Tuition assistance

Job summary

Washington University in St. Louis is seeking a Clinical Research Coordinator to manage all phases of study protocols and ensure regulatory compliance. The role involves liaison duties with the school, sponsoring agency, community and participants.

You will recruit participants, assess eligibility, obtain informed consent, and monitor study progress while coordinating data collection and reporting outcomes. This position focuses on timely protocol completion and accurate documentation.

Qualifications

• Bachelor's degree or combination of education and/or experience may substitute for minimum education.
• Basic Life Support - American Heart Association
• Basic Life Support - American Red Cross
• No specific work experience is required for this position.

Responsibilities

• Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies.
• Recruits and enrolls study participants; determines eligibility based on diagnostic criteria and/or observations.
• Develops informed consent packets and confers with participants to explain goal and obtain consent.
• Explains procedures and treatment plans; administers/tests and evaluates lab/clinical assessments for timeliness.
• Prepares presentations, reports and analyses showing progress trends and recommendations.

Skills

Clinical Research

Clinical Study Protocols

Communication

Computer Systems

Interpersonal Communication

Organizing

Research Support

Education

Bachelor's degree

Job description

Washington University in St. Louis is seeking a Clinical Research Coordinator to manage all phases of study protocols and ensure regulatory compliance. The role involves liaison duties with the school, sponsoring agency, community and participants.

You will recruit participants, assess eligibility, obtain informed consent, and monitor study progress while coordinating data collection and reporting outcomes. This position focuses on timely protocol completion and accurate documentation.