Oncology Clinical Research Coordinator (Possible Telework)

RJIT Solutions; Bethesda (MD); On-site; USD 60,000 - 90,000; Full time

Job summary

RJIT Solutions is seeking a Clinical Research Coordinator to support the NIH/NCI in Bethesda, MD. The role involves coordinating oncology trials, managing protocol activities, and maintaining regulatory documentation in a fast-paced clinical research environment.

The coordinator will screen and enroll participants, coordinate visits, collect data, and assist with audits and closeout. Strong knowledge of FDA regulations and ICH-GCP is required, with prior oncology trial experience preferred.

Qualifications

• Bachelor’s degree in a relevant field.
• Experience supporting oncology trials.
• Knowledge of FDA regulations and ICH-GCP.
• Strong organizational and communication skills.
• Experience coordinating multiple trials from startup through closeout.

Responsibilities

• Screen, pre-screen, recruit and enroll participants per protocol.
• Coordinate protocol-required visits, procedures, imaging, and labs.
• Collect, verify, and enter data; resolve sponsor and data queries; generate reports.
• Maintain regulatory documentation and study files; ensure GCP compliance.
• Assist with monitoring visits, audits, and training junior coordinators.
• Coordinate regulatory submissions, IRB documentation, and study closeout activities.

Skills

Oncology trials experience

FDA regulations knowledge

ICH-GCP

Project coordination

Strong organizational skills

Communication skills

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

Job description

RJIT Solutions is seeking a Clinical Research Coordinator to support the NIH/NCI in Bethesda, MD. The role involves coordinating oncology trials, managing protocol activities, and maintaining regulatory documentation in a fast-paced clinical research environment.

The coordinator will screen and enroll participants, coordinate visits, collect data, and assist with audits and closeout. Strong knowledge of FDA regulations and ICH-GCP is required, with prior oncology trial experience preferred.