Clinical Research Coordinator I - Diabetes Trials

University of Washington; Seattle (WA); On-site; USD 45,000 - 57,000; Full time

Job summary

The University of Washington's Department of Medicine, Division of Metabolism, Endocrinology and Nutrition, invites applications for a Research Study Coordinator 1 to join the Diabetes Institute CRU. This role focuses on coordinating clinical studies, collecting data, and managing participant involvement.

Reporting to the Research Coordinator Supervisor and Medical Director, you will follow protocols, conduct data collection, support regulatory submissions, and maintain accurate study records

Qualifications

• Two years of college coursework with two years of experience in support of clinical/biomedical/behavioral research involving human subjects.
• Equivalent education/experience may substitute for minimum qualifications.
• Excellent verbal and written communication skills; ability to multi-task.

Responsibilities

• Coordinate operations of clinical, biomedical, and behavioral studies involving human subjects.
• Support startup activities, budgets, regulatory submissions, and startup documentation.
• Coordinate specialized tasks with the research team (equipment operation, specimen processing, treatment administration).
• Perform non-invasive procedures (DXA, EKG, anthropometric measurements).
• Maintain study files compliant with FDA regulations; coordinate physician examinations and protocol adherence.
• Design data collection tools and obtain/record study data; assist in interim reports.

Skills

Multi-tasking

Verbal communication

Written communication

Data collection

Interviewing subjects

Education

Two years of college coursework

Tools

RedCap

Microsoft Excel

DXA

EKG

Job description

The University of Washington's Department of Medicine, Division of Metabolism, Endocrinology and Nutrition, invites applications for a Research Study Coordinator 1 to join the Diabetes Institute CRU. This role focuses on coordinating clinical studies, collecting data, and managing participant involvement.

Reporting to the Research Coordinator Supervisor and Medical Director, you will follow protocols, conduct data collection, support regulatory submissions, and maintain accurate study records