Registered Nurse

Elite Clinical Network

Houston (TX)

On-site

USD 39,000 - 55,000

Full time

9 days ago
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Job summary

Elite Clinical Network is seeking a compassionate and detail-oriented PRN Registered Nurse (RN) to join our growing clinical research team. This role offers a unique opportunity to contribute to groundbreaking studies across multiple therapeutic areas and gain training in a supportive environment.

Responsibilities include performing physical exams and clinical assessments per protocol, reviewing labs and ECGs, administering medications and injections when required, and maintaining accurate

Qualifications

  • Active RN license with current licensure.
  • Minimum 1 year nursing experience (clinical or research).
  • Infusion experience (IV starts, maintenance, administration).
  • Knowledge of clinical procedures, vital sign collection, and patient monitoring.
  • Strong communication, organizational, and multitasking skills.
  • Ability to work independently and in a multidisciplinary team.
  • Basic computer proficiency with Microsoft Office and EMRs/EDC systems.
  • BLS certification preferred but not required.

Responsibilities

  • Conduct physical exams and clinical assessments per protocol.
  • Review laboratory results, ECGs, 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 baseline information for clinical trial documentation.
  • Maintain accurate documentation in source documents and 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, escalating adverse events as needed.

Skills

Infusion administration
Vital signs collection
Patient monitoring
Documentation in EDC/EMR
Communication & multitasking

Education

RN license (Active)

Tools

EMRs
EDC systems
Microsoft Office

Job description

Elite Clinical Network is seeking a compassionate and detail-oriented PRN 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:

  • Active Registered Nurse (RN) license.
  • Minimum of 1 year of nursing experience (clinical or research setting).
  • Infusion experience (IV starts, maintenance, and medication administration).
  • 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.
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