Clinical Research Nurse - Oncology - Mercy Fort Smith

Find your calling at Mercy!

The Clinical Research Nurse (CRN) is responsible for coordination of research studies conducted by Mercy Research. The Clinical Research Nurse is responsible for the day-to-day operational tasks related to clinical trials and performs a variety of duties including, but not limited to, volunteer recruitment, drug / device / supply inventory maintenance, interaction with physicians, nurses, office staff, patients, and clinical monitors. Duties also include the collection, compilation, documentation and analysis of clinical research data while following local, state and federal regulations. The Clinical Research Nurse will assist in training and preceptor duties. The study load and complexity will increase from the Associate Clinical Research Nurse responsibility, thereby increasing the overall number of enrollments and visits. The Clinical Research Nurse will assist with communication and relationship building with sponsors and CROs.

Performs duties and responsibilities in a manner consistent with our mission, values, and Mercy Service Standards.

Position Details :

Clinical Research Nurse – Oncology

Location : Mercy Fort smith

Schedule : Full-Time, Day Shift

Position Overview

The Clinical Research Nurse (CRN) plays a key role in supporting oncology clinical trials at Mercy Research. This position is responsible for coordinating all aspects of research studies, including patient recruitment, informed consent, data collection, and compliance with regulatory standards. The CRN collaborates closely with physicians, nurses, office staff, patients, and clinical monitors to ensure safe, efficient, and high-quality research operations. Additional responsibilities include maintaining study drug and supply inventories, assisting with training, and fostering strong relationships with sponsors and CROs.

Key Responsibilities

• Coordinate day-to-day operations of assigned clinical trials, ensuring adherence to protocol and regulatory requirements.
• Complete pre-study feasibility assessments and checklists accurately and on time.
• Recruit and screen patients for eligibility; conduct informed consent discussions in a respectful and compliant manner.
• Manage patient visits efficiently, including monitoring, interviews, and diagnostic evaluations.
• Maintain accurate and timely documentation in case report forms and source documents.
• Prepare and process specimens for laboratory analysis.
• Educate patients on drug use, disease management, and self-monitoring.
• Maintain inventory of study drugs, devices, and supplies.
• Participate in internal quality control and compliance monitoring.
• Assist with training new staff and supporting ministry-wide recruitment efforts.
• Serve as a liaison with sponsors, CROs, and community partners to promote research and patient enrollment.
• Attend investigator meetings and training sessions as required (may involve travel).

Qualifications

Core Competencies

Why Mercy?

From day one, Mercy offers outstanding benefits - including medical, dental, and vision coverage, paid time off, tuition support, and matched retirement plans for team members working 32+ hours per pay period.

Join a caring, collaborative team where your voice matters. At Mercy, you'll help shape the future of healthcare through innovation, technology, and compassion. As we grow, you'll grow with us.