Impactful Oncology Research Coordinator (Grant-Funded)

Carilion Clinic; Roanoke (VA); On-site; USD 45,000 - 63,000; Full time

Benefits offered by this job

Medical benefits

Pension plan

Paid time off

Onsite fitness

Wellness app access

Childcare discounts

Continued education

Job summary

Carilion Clinic, Roanoke, Virginia, is seeking a Grant Funded Clinical Research Coordinator II in Oncology Research. This full-time on-site role coordinates clinical studies, ensures regulatory compliance, and actively manages study operations to support transformative cancer research.

Responsibilities include coordinating recruitment, screening, enrollment, obtaining informed consent, maintaining study documents, data management, tracking adverse events, and liaising with sponsors, IRBs, and

Qualifications

• Bachelor's degree required or 4 years of experience may be considered in lieu of degree.
• Minimum 2 years of healthcare or research experience required.
• IATA required. Research certification preferred.
• Strong analytical and organizational skills.

Responsibilities

• Coordinates recruitment, screening, and enrollment of participants.
• Obtains informed consent and manages study documentation.
• Ensures compliance with study protocols and regulatory requirements.
• Collects, manages, and analyzes study data.
• Maintains study databases and regulatory documentation.
• Tracks adverse events and protocol deviations.
• Communicates with sponsors, IRBs, and research teams.
• Supports monitoring visits and audits.

Skills

Analytical skills

Organizational skills

Education

Bachelor's degree or equivalent experience

Job description

Carilion Clinic, Roanoke, Virginia, is seeking a Grant Funded Clinical Research Coordinator II in Oncology Research. This full-time on-site role coordinates clinical studies, ensures regulatory compliance, and actively manages study operations to support transformative cancer research.

Responsibilities include coordinating recruitment, screening, enrollment, obtaining informed consent, maintaining study documents, data management, tracking adverse events, and liaising with sponsors, IRBs, and