Clinical Research Coordinator II: Multistudy Ops & Compliance

Washington University; United States; On-site; USD 55,000 - 82,000; Full time

Benefits offered by this job

Vacation time

Health insurance

Transit pass (Metro U-Pass)

Retirement plan (403(b))

Wellness programs

Caregiver leave

Tuition assistance

Job summary

Washington University in St. Louis is seeking a Clinical Research Coordinator to assist investigators across multiple studies, coordinating study protocols and liaising with the sponsor, the school, and participants.

The role involves developing plans, preparing manuscripts and grant proposals, and ensuring compliance with regulatory requirements. Responsibilities include data collection, drafting manuals, and monitoring adverse events, with opportunities to work on multiple projects and

Qualifications

• Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
• Clinical Research experience (2 years).
• Basics: BLS certification within one month of hire.

Responsibilities

• Assist in developing plans for research projects and discuss results.
• Collaborate on manuscripts and grant proposals for sponsoring agencies.
• Coordinate development of forms, questionnaires, and data collection tools.
• Maintain protocol forms, procedures, and manuals; ensure regulatory compliance.
• Monitor participant progress and report adverse events; liaise with funding agencies.

Skills

Clinical Research

Data interpretation

Manuscripts preparation

Grant proposals

Statistical analysis software

Education

Bachelor’s degree

Tools

SAS

Job description

Washington University in St. Louis is seeking a Clinical Research Coordinator to assist investigators across multiple studies, coordinating study protocols and liaising with the sponsor, the school, and participants.

The role involves developing plans, preparing manuscripts and grant proposals, and ensuring compliance with regulatory requirements. Responsibilities include data collection, drafting manuals, and monitoring adverse events, with opportunities to work on multiple projects and