Oncology Clinical Research Nurse — Trial Coordination

Georgetown University; United States; On-site; USD 55,000 - 100,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

Disability and life insurance

Retirement savings

Tuition assistance

Work-life balance benefits

Employee discounts

Job summary

Georgetown University’s Lombardi Comprehensive Cancer Center seeks a Clinical Research Nurse 1 (CRN 1) to lead the coordination of oncology clinical trials within the Lombardi Clinical Trials Office. You will recruit participants, obtain informed consent, perform trial procedures, and ensure patient safety in accordance with GCP.

You will support study coordinators, manage data in CTMS, and liaise with investigators, IRB, sponsors, and auditors while ensuring regulatory compliance across the

Qualifications

• Bachelor’s degree, BLS certification, and RN license in the District of Columbia.
• 3–5 years nursing experience in a hospital, clinic, or similar health care setting.
• Preference for inpatient/ICU settings.
• At least 1 year of clinical research experience preferred.
• At least 1 year of oncology experience preferred.
• Knowledge of clinical research, Good Clinical Practice (GCP).
• Excellent verbal and written communication, organizational skills, and attention to detail.
• Reliable and able to prioritize competing responsibilities.

Responsibilities

• Coordinate the overall trial lifecycle for assigned clinical trials.
• Participate in recruitment and selection of study participants; document data to support screening.
• Interface with participants to obtain informed consent per protocol and policies.
• Coordinate or conduct study-related procedures while maintaining protocol integrity and patient safety per GCP.
• Assist in care continuum across outpatient, inpatient, and home settings; triage calls and symptom management.
• Document all study activity in medical records and patient research charts.
• Follow-up with participants as per standards and protocols.
• Provide nursing support to CRNs and other CRCs.
• Ensure site compliance with research protocols by reviewing regulatory requirements.
• Coordinate collection of research specimens per protocol requirements.
• Educate patients about clinical trial participation and required testing.
• Schedule and conduct in-service training for staff on trials.
• Update CTMS with patient information and key dates to support study management.
• Collaborate with Data Coordinators to ensure complete and accurate documentation.

Skills

RN license

BLS certification

Bachelor's degree

Clinical research experience

Regulatory knowledge

Communication skills

Education

Bachelor's degree in nursing

Tools

CTMS

Job description

Georgetown University’s Lombardi Comprehensive Cancer Center seeks a Clinical Research Nurse 1 (CRN 1) to lead the coordination of oncology clinical trials within the Lombardi Clinical Trials Office. You will recruit participants, obtain informed consent, perform trial procedures, and ensure patient safety in accordance with GCP.

You will support study coordinators, manage data in CTMS, and liaise with investigators, IRB, sponsors, and auditors while ensuring regulatory compliance across the