Temp IV Infusion Nurse

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 youre 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 systemsBLS certification preferred but not required

• 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