Cardiovascular Research Program Coordinator

Virginia Commonwealth University School of Medicine; Richmond (VA); On-site; USD 55,000 - 62,000; Full time

Benefits offered by this job

Health benefits

Tuition benefits

Paid leave

Job summary

Virginia Commonwealth University School of Medicine in Richmond seeks a Clinical Research Coordinator to support a high-volume cardiovascular program. The role coordinates study startup, regulatory tasks, data management, and manuscript preparation, while fostering collaboration among investigators, staff, and sponsors.

The position emphasizes regulatory compliance, study logistics, and training of trainees, with full onsite work and a strong emphasis on team-based program development.

Qualifications

• Bachelor's degree or 3 years in clinical/research environment.
• Strong organizational skills and ability to manage multiple priorities.
• Excellent written and verbal communication; collaboration with multidisciplinary teams.
• Proficiency with Microsoft Office and research systems.

Responsibilities

• Coordinate clinical research operations and study activities.
• Serve as liaison among managers, investigators, sponsors, and staff.
• Assist startup/activation of new studies and ensure readiness.
• Manage participant scheduling, visits, and study logistics.
• Coordinate meetings to support planning and collaboration.
• Monitor progress, enrollment goals, and timelines; escalate barriers.
• Provide program support for regulatory, fiscal, and scholarly activities.

Skills

Strong organizational skills

Excellent written and verbal沟通

Ability to manage multiple priorities

Attention to detail

Team collaboration

Education

Bachelor's degree in health sciences, biological or behavioral sciences, public health, nursing, or related program

Tools

Microsoft Office Suite

Job description

Virginia Commonwealth University School of Medicine in Richmond seeks a Clinical Research Coordinator to support a high-volume cardiovascular program. The role coordinates study startup, regulatory tasks, data management, and manuscript preparation, while fostering collaboration among investigators, staff, and sponsors.

The position emphasizes regulatory compliance, study logistics, and training of trainees, with full onsite work and a strong emphasis on team-based program development.