Cardiovascular Clinical Research Coordinator: Impact

University of Virginia; Charlottesville (VA); On-site; USD 55,000 - 85,000; Full time

Benefits offered by this job

Restaurant? Not listed

Job summary

University of Virginia’s Division of Cardiovascular Medicine is seeking Clinical Research Coordinators of varying levels to join a dynamic team in Charlottesville. The CRC will coordinate studies from start-up to archival, work with physicians and staff, and ensure regulatory compliance across clinical trials in heart disease and related conditions.

Responsibilities include consent, data collection, documentation, and logistics across inpatient, outpatient, and lab settings.

Qualifications

• Bachelor's Degree required or equivalent combination of experience, education, and/or certifications.
• CRC levels vary by experience: CRC1–no required experience; CRC4–7+ years.

Responsibilities

• Recruitment, screening, and enrolling study participants who meet research criteria.
• Collect basic information through scripted and non-scripted interviews.
• Planning and executing tasks.
• Organizational and planning tasks.
• Attention to detail in data handling and documentation.
• Problem-solving to address protocol and regulatory questions.
• Excellent verbal and written communication with team and participants.
• Obtaining informed consent and maintaining contact with participants.
• Collection of subject data, logs, tracking participants, preparing study materials.
• Processing, preparing and shipping laboratory specimens.
• Other duties may be assigned related to trials.

Skills

Recruitment

Consent

Data collection

Documentation

Communication

Problem solving

Attention to detail

Education

Bachelor's Degree

Job description

University of Virginia’s Division of Cardiovascular Medicine is seeking Clinical Research Coordinators of varying levels to join a dynamic team in Charlottesville. The CRC will coordinate studies from start-up to archival, work with physicians and staff, and ensure regulatory compliance across clinical trials in heart disease and related conditions.

Responsibilities include consent, data collection, documentation, and logistics across inpatient, outpatient, and lab settings.