Clinical Research Data Coordinator (Hybrid) – EMR/EDC Specialist

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

Benefits offered by this job

Vacation, holidays, sick time

Health insurance

Metro transit U-Pass

Retirement savings plan

Job summary

Washington University in St. Louis is seeking a Data Coordinator to support clinical research trials by extracting data from EMR and other sources into an EDC system. The role may involve multiple trials and requires meticulous data collection and coordination with the study team, sponsors, and vendors.

The ideal candidate has a Bachelor’s degree (or equivalent) with familiarity in clinical research procedures, data management, and regulatory compliance. The position is based in St.

Qualifications

• Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
• Basic Life Support certification required within one month of hire date.
• SOCRA/ACRP certification optional depending on department.

Responsibilities

• Works under PI guidance to meet project objectives.
• Assists with study start-up activities including IRB applications.
• Identifies, screens, and enrolls study subjects.
• Ensures protocol requirements are met and coordinates study procedures.
• Handles, processes, and ships research specimens; organizes source documentation.
• Prepares/submits reportable event reports to sponsors and IRB.
• Collaborates with sponsor teams during monitoring and provides documentation.

Skills

Clinical Research

Data Entry

Communication

Interpersonal Communication

Organizing

Research Support

Education

Bachelor’s degree

Tools

EMR

EDC system

Job description

Washington University in St. Louis is seeking a Data Coordinator to support clinical research trials by extracting data from EMR and other sources into an EDC system. The role may involve multiple trials and requires meticulous data collection and coordination with the study team, sponsors, and vendors.

The ideal candidate has a Bachelor’s degree (or equivalent) with familiarity in clinical research procedures, data management, and regulatory compliance. The position is based in St.