Oncology Clinical Research Coordinator I - Day Shift

Inova Health; Virginia (MN); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Medical, dental and vision coverage

Tuition and student loan assistance

Mental health support

Paid time off & parental leave

Flexible work schedules

Job summary

Inova Schar Cancer Research is seeking a Clinical Research Coordinator 1 - Oncology to join our team in Fairfax, VA. This full-time, day-shift role supports study coordination from site selection through closure and handles financial aspects of study implementation under supervision.

The role emphasizes GCP-aligned study activities, subject protection, and collaboration with multidisciplinary teams in a leading oncology research environment.

Qualifications

• Associate's Degree or relevant experience in lieu of a degree.
• 2 years of patient care experience or 1 year of clinical research experience with a Bachelor's Degree.

Responsibilities

• Identifies and explains key protocol elements and performs study tasks under direct supervision.
• Explains basic elements of subject safety including IRB/IEC rationale, study activity documentation, and event reporting requirements.
• Demonstrates subject protection under direct supervision.
• Explains the investigational products development process and key regulations.
• Explains and performs study operational activities in GCP and non-GCP study management.
• Explains how to document data according to ALCOA-C principles.
• Explains the importance of professional conduct and leadership principles affecting site operations.
• Explains communication channels and outlets for study results affecting conduct of clinical research.
• May perform other duties as assigned.

Skills

Clinical research

Patient care

Informed consent

Team collaboration

Education

Associate's Degree or equivalent experience

Job description

Inova Schar Cancer Research is seeking a Clinical Research Coordinator 1 - Oncology to join our team in Fairfax, VA. This full-time, day-shift role supports study coordination from site selection through closure and handles financial aspects of study implementation under supervision.

The role emphasizes GCP-aligned study activities, subject protection, and collaboration with multidisciplinary teams in a leading oncology research environment.