Position Overview
We are seeking a compassionate and detail-oriented Registered Nurse (RN) to join our growing clinical research team. 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.