Hybrid Clinical Research Coordinator - Data & Patient Impact

Vcu Rrtc; Richmond (VA); Hybrid; USD 24,796 - 41,328; Full time

Benefits offered by this job

Hybrid work arrangement

Job summary

VCU Health in Richmond, VA seeks a Clinical Research Coordinator to support study conduct, data management, and regulatory compliance across multiple studies. You will assist with recruitment, informed consent, enrollment, and ongoing participant monitoring, ensuring adherence to GCP, HIPAA, and IRB requirements.

The role also involves data entry into sponsor CRFs and OnCore, maintaining audit-ready study files, handling sponsor queries, and coordinating study documentation alongside the PI and

Qualifications

• Must have ability to prioritize work and multi-task in fast-paced environment.
• Flexibility with working hours and shift requirements.
• Professionalism and ability to work independently and as a team.
• Establish and maintain productive relationships with VCU colleagues and stakeholders.
• Must be dependable, detail-oriented, and accurate.

Responsibilities

• Study Conduct: assist in recruitment, enrollment, consent, monitor patients, identify potential participants, coordinate and file documents.
• Data Management: enter study data, maintain audit-ready files, and handle sponsor CRFs and databases in OnCore.
• Regulatory & Compliance: ensure protocol compliance, maintain study docs, IRB submissions and training logs.
• General/Admin: cross-coverage across studies, scheduling, filing, ordering study materials, and follow procedures.

Skills

Prioritize work

Multi-tasking

Professionalism

Relationship building

Attention to detail

Reading & applying regulations

Organization & time management

Critical thinking

Team collaboration

Education

Bachelor’s Degree or equivalent in sciences

Tools

RedCap

EPIC

OnCore

Microsoft Programs

Job description

VCU Health in Richmond, VA seeks a Clinical Research Coordinator to support study conduct, data management, and regulatory compliance across multiple studies. You will assist with recruitment, informed consent, enrollment, and ongoing participant monitoring, ensuring adherence to GCP, HIPAA, and IRB requirements.

The role also involves data entry into sponsor CRFs and OnCore, maintaining audit-ready study files, handling sponsor queries, and coordinating study documentation alongside the PI and