Surgery Oncology: Clinical Research Coordinator I

Washington University in St. Louis; Missouri; Hybrid; USD 49,000 - 74,000; Full time

Benefits offered by this job

Paid time off

Holiday pay

Health insurance

Metro U-Pass transit benefits

403(b) retirement plan

Wellness resources

Caregiver leave

Tuition assistance

Job summary

Washington University in Saint Louis is seeking a Clinical Research Coordinator I for Surgery Oncology. The role coordinates multiple clinical studies, ensuring protocol compliance and quality data collection with interface to investigators, sponsors, and participants.

The position involves recruiting participants, obtaining informed consent, scheduling procedures, and communicating findings to the care team, while supporting study integrity and regulatory adherence.

Qualifications

• Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
• Basic Life Support (BLS) certification required.
• No specific work experience is required for this position.

Responsibilities

• Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and regulatory requirements.
• Recruits and enrolls study participants; assesses eligibility and obtains informed consent.
• Ensures timely completion of protocol requirements including scheduling, testing, and data collection.
• Maintains data accuracy, prepares reports, and communicates progress to stakeholders.
• Acts as liaison with funding or sponsoring agency and investigators.

Skills

Clinical Research

Clinical Study Protocols

Communication

Computer Systems

Interpersonal Communication

Organizing

Research Support

Education

Bachelor’s degree

Job description

Washington University in Saint Louis is seeking a Clinical Research Coordinator I for Surgery Oncology. The role coordinates multiple clinical studies, ensuring protocol compliance and quality data collection with interface to investigators, sponsors, and participants.

The position involves recruiting participants, obtaining informed consent, scheduling procedures, and communicating findings to the care team, while supporting study integrity and regulatory adherence.