Oncology Clinical Research Coordinator II - Data & Protocols

Washington University in St. Louis; St. Louis (MO); On-site; USD 55,000 - 82,000; Full time

Job summary

Washington University in St. Louis is seeking a Data Coordinator to support multiple clinical research trials by extracting data from EMR and other sources and entering it into an EDC system.

You will coordinate data collection, ensure accuracy, and act as a liaison among the clinic, sponsors, vendors, and study team. Responsibilities include developing study plans, creating forms, managing protocol amendments, and monitoring data quality across all study phases to ensure safety and compliance.

Qualifications

• Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
• SOCRA/ACRP certification is optional depending on department.
• Clinical Research experience (2 years) noted in posting.
• No specific license required for this position.

Responsibilities

• Assist in developing plans for research projects and interpretation of results.
• Coordinate forms, questionnaires and manuals for study progress and data collection.
• Implement and manage all phases of study/protocol, ensuring regulatory compliance.
• Analyze data and prepare progress reports and recommendations.
• Serve as liaison with sponsors, vendors and the study team.

Skills

Clinical Research

Clinical Study Protocols

Database Management

Research Projects

Spreadsheet Analysis

SAS

Education

Bachelor's degree

Tools

SAS

Job description

Washington University in St. Louis is seeking a Data Coordinator to support multiple clinical research trials by extracting data from EMR and other sources and entering it into an EDC system.

You will coordinate data collection, ensure accuracy, and act as a liaison among the clinic, sponsors, vendors, and study team. Responsibilities include developing study plans, creating forms, managing protocol amendments, and monitoring data quality across all study phases to ensure safety and compliance.