Oncology Clinical Research Coordinator (Telework Eligible)

RJ IT Solutions; Bethesda (MD); On-site; USD 70,000 - 110,000; Full time

Job summary

RJIT Solutions seeks a Clinical Research Coordinator to support the National Cancer Institute (NCI) Office of the Clinical Director at the NIH Clinical Center in Bethesda, MD. The role covers protocol activation, participant screening, data management, regulatory documentation, and multi-study coordination in oncology trials, ensuring FDA/ICH-GCP compliance.

The ideal candidate brings hands-on oncology trial experience, familiarity with EMR/CTMS/EDC systems, and strong organizational skills to

Qualifications

• A Bachelor's degree in Nursing, Biological Sciences, Public Health, Health Sciences, Clinical Research, or a related field is required.
• Demonstrated experience supporting clinical trials from startup through closeout, with oncology clinical trials experience and clinical research operations.

Responsibilities

• Coordinate protocol activation, visits, procedures, specimens, and imaging across multiple oncology trials.
• Collect, review, and validate research data in approved electronic systems; ensure data quality and completeness.
• Maintain regulatory binders, study files, and source documentation; support IRB submissions and study closeout.
• Assist with training junior staff and ensuring compliance with FDA regulations, ICH-GCP, and sponsor requirements.

Skills

Oncology trials experience

FDA regulations familiarity

ICH-GCP knowledge

Data coordination

Education

Bachelor's degree in Nursing, Biological Sciences, Public Health, Health Sciences, Clinical Research, or related field

Tools

EMR systems

CTMS

EDC platforms

Microsoft Office Suite

Job description

RJIT Solutions seeks a Clinical Research Coordinator to support the National Cancer Institute (NCI) Office of the Clinical Director at the NIH Clinical Center in Bethesda, MD. The role covers protocol activation, participant screening, data management, regulatory documentation, and multi-study coordination in oncology trials, ensuring FDA/ICH-GCP compliance.

The ideal candidate brings hands-on oncology trial experience, familiarity with EMR/CTMS/EDC systems, and strong organizational skills to