Registered Nurse

Elite Clinical Network; Sun City (AZ); On-site; USD 65,000 - 85,000; Full time

Job summary

A healthcare organization in Sun City is seeking a compassionate Registered Nurse (RN) to join its clinical research team. This role offers the chance to conduct physical exams, assist in medication administration, and ensure patient safety during clinical trials. Candidates should have at least 1 year of nursing experience and excellent communication skills. The team provides training for those transitioning to this exciting field. Join us to contribute to groundbreaking research studies across various therapeutic areas.

Qualifications

• Minimum of 1 year of nursing experience in a clinical or research setting.
• Strong understanding of clinical procedures and patient monitoring.
• BLS certification preferred but not required.

Responsibilities

• Conduct physical exams and clinical assessments on study participants.
• Review laboratory results and report abnormalities.
• Assist with medication administration and maintain accurate documentation.
• Collaborate with study teams to ensure compliance with protocols.

Skills

Compassion

Attention to detail

Organizational skills

Communication skills

Multitasking

Tools

Microsoft Office

EMR systems

EDC systems

Job description

Elite Clinical Network is seeking a compassionate and detail-oriented Registered Nurse (RN) to join our growing clinical research. This role offers a unique opportunity to contribute to groundbreaking research studies across multiple therapeutic areas. Whether you're experienced in research or transitioning from a clinical setting, we provide training to help you succeed in this exciting field.

Key Responsibilities

• Conduct physical exams and clinical assessments on study participants per protocol.
• Review laboratory results, ECGs, and other clinical findings and report abnormalities to the Principal Investigator.
• Assist with medication administration, including injections and infusions when required by study protocol.
• Collect vital signs, medical histories, and other baseline information as needed for clinical trial documentation.
• Maintain accurate and timely documentation in source documents and electronic data capture (EDC) systems.
• Collaborate with study coordinators, investigators, and other research staff to ensure compliance with protocols, GCP, and regulatory standards.
• Assist in maintaining study supplies and investigational product accountability.
• Participate in monitoring visits, audits, and site initiation or close-out visits as necessary.
• Ensure patient safety and comfort, identifying and escalating any adverse events or deviations.

Qualifications

• Minimum of 1 year of nursing experience (clinical or research setting).
• Strong understanding of clinical procedures, vital sign collection, and patient monitoring.
• Excellent communication, organizational, and multitasking skills.
• Ability to work independently and as part of a multidisciplinary team.
• Basic computer proficiency including Microsoft Office and familiarity with EMRs or EDC systems.
• BLS certification (preferred but not required).

Preferred Experience (Not Required)

• Prior experience in clinical research, pharma trials, or investigational drug studies.
• Knowledge of ICH-GCP guidelines and FDA regulations.
• Familiarity with clinical trial protocols and informed consent procedures.