Research Nurse - Per Diem

Adams Clinical•New York, NY

3h•$55 - $65•Onsite

About The Position

Adams Clinical is seeking a per diem, as-needed Registered Nurse to provide on-site clinical support at its clinical research site in The Bronx. The nurse works under the direction of physician Principal Investigators and Clinical Operations leadership, supporting pharmaceutical-sponsored clinical trials in accordance with study protocols, FDA regulations, Good Clinical Practice (GCP) guidelines, and applicable research requirements. Typical duties include injections, investigational product preparation, IV catheterization and drug infusion, phlebotomy, medical-record and clinical-results review, medication reconciliation, and medical liaison work. The role requires comfort in a clinical research environment, adherence to study protocols, and clear, timely documentation. Hours vary according to clinical and study needs. Pay is $55–$65 per hour, commensurate with experience.

Requirements

Current, unrestricted Registered Nurse license in the state of New York.
Bachelor’s degree in nursing (BSN).
Recent bedside nursing experience.
Strong attention to detail and ability to follow study protocols and established clinical procedures while maintaining clear, accurate, and timely clinical documentation.
Strong communication and collaboration skills, including the ability to work effectively with Principal Investigators, sub-Investigators, Clinical Research Coordinators, and other study team members.

Nice To Haves

Two or more years of nursing experience.
Strong IV placement, phlebotomy, and infusion skills.
Previous clinical research experience and familiarity with GCP and FDA regulations.
BLS/CPR certification.

Responsibilities

Support preparation and handling of investigational product (IP), as permitted by study protocols, site procedures, and applicable requirements.
Administer subcutaneous and intramuscular injections in accordance with study protocols and nursing scope of practice.
Place IVs and initiate and monitor IV infusions in accordance with study protocols and nursing scope of practice.
Perform phlebotomy and assist with difficult blood draws.
Assist with collecting vital signs and other protocol-required clinical assessments.
Identify and escalate clinically significant findings, changes in participant condition, and potential reactions to study dosing in collaboration with the site Principal Investigator.
Review medical records and reconcile relevant information with participant-reported history in collaboration with site medical investigators.
Assist with collecting and documenting adverse events, concomitant medications, and medical history.
Assist with identifying, documenting, and reporting Serious Adverse Events, including required regulatory and IRB documentation.
Support participant safety and respond appropriately to urgent or emergency clinical situations within nursing scope of practice and site procedures, including assisting with crash cart supply and medication checks as needed.
Document clinical procedures and participant-related information accurately and promptly in accordance with study protocols and applicable requirements.
Collaborate with Principal Investigators, medical sub-Investigators, Clinical Operations, Clinical Research Coordinators, and other study team members to support safe and efficient study conduct.