Registered Nurse

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.
• Absorb and maintain 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

• 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.

Pay

$35-50/hr