Registered Nurse (RN) - Research Nurse I

Dartmouth-Hitchcock Health; Lebanon (NH); On-site; USD 65,000 - 90,000; Full time

Job summary

Dartmouth-Hitchcock Health seeks a Clinical Research Nurse I to support inpatient and outpatient participants in investigational therapy trials. Under PI supervision, you will provide care, education, and coordination throughout the trial process in collaboration with the research team.

This entry-level role requires nursing licensure in NH, strong communication, attention to detail, and a willingness to learn Good Clinical Practice standards; prior research experience is preferred but not

Qualifications

• Graduate from an accredited nursing school.
• Bachelor of Science in Nursing preferred; must be obtained within 4 years of hire.
• Minimum of 2 years clinical nursing experience.
• Excellent interpersonal and communication skills.
• Excellent attention to detail.

Responsibilities

• Provide patient care to inpatients and outpatients receiving investigational therapy.
• Screen and recruit potential research participants and assist with eligibility screening.
• Educate patients and families regarding investigational therapy with the medical team.
• Ensure patients are scheduled for all study assessments per protocol.
• Assist with preparation and administration of medications per protocol.
• Assist with evaluation and management of drug- and disease-related toxicities and symptoms.
• Utilize electronic systems for study operations and data documentation.
• Assist with data collection documents and instruments and maintain data security.

Skills

Clinical nursing

Interpersonal communication

Attention to detail

Team collaboration

Data documentation

Education

Bachelor of Science in Nursing

RN licensure / NH eligibility

Job description

Overview

The Clinical Research Nurse I performs a variety of clinical and non-clinical tasks associated with conducting clinical research, and within the scope of licensure. Working closely with research participants and their families, they provide care, education and support throughout the trial. Under the supervision of the PI or their designee, this position collaborates with research and non-research staff, maintaining involvement throughout the clinical trial process. The role of the Clinical Research Nurse I is introductory, with assignments provided at a task level, and focused on less complex clinical research trials and processes.

Responsibilities

Research Operations

• Provide patient care to inpatients and outpatients receiving investigational therapy
• Screen and recruit potential research participants and assist with verification of inclusion and exclusion criteria for eligibility purposes
• Assist with educating patients and families regarding investigational therapy in collaboration with the medical team
• Ensure that patients are scheduled for all study assessments as required per research protocol
• Assist with the preparation and administration of all medications required per research protocol, including investigational and standard of care agents
• Assist with the evaluation and management of research patients for drug and/or disease-related toxicities and symptoms

Ethics & Participant Safety:

• Adhere to and maintain Good Clinical Practice (GCP)/Human Subjects Protection (HSP) practices and required training
• Articulate the rationale for individual protocols
• Serve as a resource to ensure staff and patients recognize the difference between routine clinical care management and care management of clinical research participants

Data and Informatics

• Utilize electronic systems, technologies, and software necessary for study operations
• Accurately document study visit assessments for data collection And assist with data entry as needed
• Assist with the development of, data collection documents and instruments
• Adhere to required processes, policies, and systems protocols to ensure data security

Leadership and Professionalism

• Follow professional guidelines and code of ethics related to the conduct of clinical research.

Site and Study Management

• Assist in the initiation, management, and completion of clinical trials and research studies.
• Perform other duties as assigned, such as supporting regulatory affairs

Communication and Team

• Collaborate with and educates healthcare professionals regarding investigational research protocols
• Ensure research compliance and adherence to protocol guidelines

Clinical Skills

• Ensure a safe, effective, and efficient patient care environment
• Facilitate and monitor activities related to the delivery of patient care within research
• Other duties as assigned

Qualifications

• Graduate from an accredited nursing school required.
• Bachelor of Science in Nursing preferred. Must be obtained within 4 years of hire
• Previous knowledge of research preferred
• Minimum of 2 years clinical nursing experience required
• Excellent interpersonal and communication skills required
• Excellent attention to detail required

Required Licensure/Certifications

• Licensed Registered Nurse with NH Eligibility
• Basic Life Support (BLS) certification required
• Human Subjects Protection (HSP) within 30 days
• Certified Good Clinical Practice (CGCP) within 30 days
• Responsible Conduct in Research (RCR) within 30 days