Welcoming you to Endless Opportunities

1. Assist principal investigators with protocol review and development
2. Collaborate on quality assurance and protocol-specific materials

1. Recruit and register patients for clinical trials
2. Coordinate scheduling of labs, imaging, admissions, and visits
3. Collaborate with coordinators and disease group staff to complete trials

1. Coordinate study enrollment, treatment, and study requirements
2. Collaborate with care teams including infusion, radiation, and surgical nurses
3. Educate patients and families on protocols, adapting to age and cultural needs
4. Order and monitor specimens and administer medications as necessary
5. Document in charts and communicate findings to investigators and physicians
6. Provide protocol training and serve as a resource to the healthcare team
7. Monitor patient safety and regulatory compliance

1. Identify areas for growth and set professional goals
2. Engage in professional organizations locally and nationally
3. Participate in committees and prepare reports, articles, and presentations
4. 
   

1. Current Registered Nurse license
2. Bachelor of Science in Nursing (BSN) preferred; Associate Degree accepted
3. Experience in clinical research and oncology
4. Strong communication, organizational, and patient care skills

1. Prior experience in cancer clinical trials
2. Familiarity with regulatory compliance and trial activation

Education: Masters Degree