Clinical Research Coordinator I – Day Shift (Fairfax, VA)

Inova; Fairfax (VA); On-site; USD 45,000 - 70,000; Full time

Benefits offered by this job

Medical, dental and vision coverage

Retirement match (5%)

Tuition and student loan assistance

Mental health support for team and/dep

Flexible work schedules; paid time off

Job summary

Inova Health is seeking a dedicated Clinical Research Coordinator 1 for the Inova Saville Cancer Screening and Prevention Research program in Fairfax, VA. This full-time, day-shift role runs Monday through Friday in a hospital-based setting.

You will support study coordination from site selection through closure, ensuring human subject protection, protocol feasibility, and study documentation under supervision.

Qualifications

• Education: Associate degree (or relevant experience in lieu of degree)
• Experience: 2 years of patient care experience or 1 year 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 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 compliance with GCP and non-GCP study management.
• Documents data according to ALCOA-C principles.
• Explains professional conduct and leadership principles for investigative site operations.
• Outlines various communication channels and outlets for study results.

Skills

Patient care

Clinical research

GCP/IRB basics

Education

Associate degree

Tools

Epic EHR

REDCap

Job description

Inova Health is seeking a dedicated Clinical Research Coordinator 1 for the Inova Saville Cancer Screening and Prevention Research program in Fairfax, VA. This full-time, day-shift role runs Monday through Friday in a hospital-based setting.

You will support study coordination from site selection through closure, ensuring human subject protection, protocol feasibility, and study documentation under supervision.