Cancer Research Coordinator I: Day Shift & Impact

Inova; Fairfax (VA); On-site; USD 55,000 - 85,000; Full time

Benefits offered by this job

Health insurance

Retirement plan

Education assistance

Mental health support

Work-life balance

Job summary

Inova Saville Cancer Screening and Prevention Research is seeking a dedicated Clinical Research Coordinator 1 to join their Fairfax, VA team. This full-time, day-shift role covers study coordination from site selection through closure, with responsibilities across protocol feasibility to study activities under supervision.

The role emphasizes understanding of subject safety, IRB/IEC processes, data documentation (ALCOA-C), and collaboration with multidisciplinary teams in hospital and community

Qualifications

• 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 including IRB/IEC requirements, study activity documentation, and event reporting requirements.
• Explains the investigational products development process and key regulations to control these processes.
• Explain and perform study operational activities in compliance with Good Clinical Practice (GCP) and non-GCP related study management activities.
• Document data according to ALCOA-C principles.
• Describe leadership principles that impact the effective operation of an investigative site.
• Describe the variety of communication channels and outlets for study results that impact the conduct of clinical research.
• May perform other duties as assigned.

Skills

Clinical research coordination

Good Clinical Practice (GCP)

Epic EHR

REDCap

Tools

Epic EHR

REDCap

Job description

Inova Saville Cancer Screening and Prevention Research is seeking a dedicated Clinical Research Coordinator 1 to join their Fairfax, VA team. This full-time, day-shift role covers study coordination from site selection through closure, with responsibilities across protocol feasibility to study activities under supervision.

The role emphasizes understanding of subject safety, IRB/IEC processes, data documentation (ALCOA-C), and collaboration with multidisciplinary teams in hospital and community