Clinical Research Coordinator II: Study Operations

Washington University in St. Louis; United States; On-site; USD 55,000 - 82,000; Full time

Job summary

Washington University in St. Louis invites applications for a Clinical Research Coordinator position in Saint Louis, MO.

The role assists investigators across a complex study portfolio, liaising with the university, sponsors, and participants while overseeing protocol compliance throughout all study phases. The ideal candidate holds a bachelor’s degree or equivalent experience, with at least two years in clinical research and BLS certification within one month of hire.

Qualifications

• Bachelor's degree or combination of education and/or experience may substitute for minimum education.
• Basic Life Support certification must be obtained within one month of hire date.
• Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirement).
• Clinical research experience, minimum 2 years.
• No additional education unless stated elsewhere in the job posting.

Responsibilities

• Assist in developing plans for research projects and discuss interpretation of results; help prepare manuscripts and grant proposals.
• Coordinate development of forms and procedures; assist in writing manuals for study progress and data collection.
• Manage all phases of study protocol; ensure compliance with regulations; maintain records and report adverse events.
• Evaluate and interpret collected clinical data; prepare presentations and analyses with progress trends and recommendations.
• Perform other duties as assigned.

Tools

Clinical Research

Clinical Study Protocols

Database Management

Research Projects

Spreadsheet Analysis

SAS

Job description

Washington University in St. Louis invites applications for a Clinical Research Coordinator position in Saint Louis, MO.

The role assists investigators across a complex study portfolio, liaising with the university, sponsors, and participants while overseeing protocol compliance throughout all study phases. The ideal candidate holds a bachelor’s degree or equivalent experience, with at least two years in clinical research and BLS certification within one month of hire.