Oncology Clinical Research Coordinator I (Day Shift)

Inova Health System; Fairfax (VA); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Medical, dental and vision coverage

Retirement matching

Student loan assistance

Mental health support

Paid time off and parental leave

Job summary

Inova Schar Cancer Research in Fairfax, VA seeks a Clinical Research Coordinator 1 - Oncology to join its team. This full-time, day-shift role supports study coordination from site selection through closure and ensures human subject protection.

The role involves explaining protocol elements, assisting with regulatory tasks, and coordinating study activities under supervision, with opportunities to grow in clinical research and work with multidisciplinary teams.

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 requirements, study activity documentation, and event reporting requirements.
• Explains the investigational products development process and key regulations to control these processes.
• Explains and performs study operational activities in compliance with GCP and non-GCP study management activities.
• Explains how to document data according to ALCOA-C principles.
• Explains the importance of professional conduct and leadership principles at an investigative site.
• May perform other duties as assigned.

Skills

Patient care

Clinical research

Education

Associate’s degree

Job description

Inova Schar Cancer Research in Fairfax, VA seeks a Clinical Research Coordinator 1 - Oncology to join its team. This full-time, day-shift role supports study coordination from site selection through closure and ensures human subject protection.

The role involves explaining protocol elements, assisting with regulatory tasks, and coordinating study activities under supervision, with opportunities to grow in clinical research and work with multidisciplinary teams.