Registered Nurse

Career Opportunities with ECN Operating LLC

A great place to work.

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.

• 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.

• 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).

• 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
  .