Oncology Clinical Research Nurse
2 weeks ago
Oncology Clinical Research Nurse - Lombardi Comprehensive Cancer Center
Join a dedicated team at the Lombardi Comprehensive Cancer Center, where we are committed to advancing cancer treatment through innovative research and compassionate patient care. Our institution fosters a collaborative environment aimed at improving health outcomes and supporting the community.
Position Overview
As an Oncology Clinical Research Nurse, you will play a vital role in managing phase I, II, and III oncology clinical trials. Your responsibilities will encompass:
- Overseeing the comprehensive coordination of assigned clinical trials from initiation to completion.
- Collaborating with principal investigators and senior team members in the recruitment and selection of study participants, ensuring adherence to eligibility criteria.
- Engaging with study participants to obtain informed consent in accordance with established protocols and regulatory standards.
- Conducting study-related procedures and assessments while prioritizing patient safety and protocol fidelity, adhering to Good Clinical Practice (GCP) guidelines.
- Facilitating the continuum of care, including managing patient communications and symptom management.
- Documenting all trial-related activities, including medical data, in compliance with protocol and sponsor requirements.
- Following up with study participants in alignment with established protocols.
- Providing clinical and administrative support to the Clinical Research Coordinator and other nursing staff.
- Ensuring compliance with research protocols by reviewing regulatory requirements and implementing appropriate practices.
- Coordinating the collection of research specimens in line with protocol specifications.
- Educating patients about clinical trial participation, potential treatments, side effects, and necessary testing.
- Conducting training sessions for staff involved in clinical trials.
- Maintaining the Clinical Trials Management System (CTMS) with accurate patient information and key dates.
- Collaborating with Data Coordinators to ensure complete and accurate documentation for clinical trials.
- Reporting serious adverse events as per protocol and institutional policies.
- Acting as a liaison with hospital staff, physicians, and regulatory bodies.
- Identifying and addressing barriers to patient and physician participation in clinical trials.
- Participating in relevant meetings and committees as assigned.
- Adhering to all applicable laws, regulations, and institutional policies.
- Complying with Human Subject Protection and maintaining patient confidentiality.
Work Environment
This position is designated as On-Campus. Work mode designations are regularly reviewed to meet the evolving needs of the institution.
Qualifications
- Bachelor's degree, BLS certification, and RN license required.
- 3 to 5 years of nursing experience in a healthcare setting, with a preference for clinical research experience.
- Strong candidates will demonstrate knowledge of clinical research, GCP, and possess excellent communication and organizational skills.
Compensation
The anticipated salary range for this position is between $54,000 and $100,493.33, influenced by individual qualifications and experience.
Equal Opportunity Statement
We are an Equal Opportunity/Affirmative Action Employer, dedicated to fostering a diverse workforce. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, age, sex, disability status, or any other characteristic protected by law.
Benefits
We offer a comprehensive benefits package, including medical, dental, vision, and retirement savings options, along with professional development opportunities and work-life balance initiatives.
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