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.