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.
