Research Nurse - Per Diem

Adams Clinical•Philadelphia, PA

3h•$45 - $55•Onsite

About The Position

Adams Clinical is seeking a per diem PRN Registered Nurse to provide flexible, as-needed, on-site clinical support at its clinical research site in Philadelphia. The role works under the direction of physician Principal Investigators and Clinical Operations leadership to conduct pharmaceutical-sponsored clinical trials in accordance with study protocols, FDA regulations, GCP guidelines, and applicable research requirements. Typical tasks include injections, investigational product preparation, IV catheterization and drug infusion, phlebotomy, medical record and clinical results review, medication reconciliation, and medical liaising. The nurse must be comfortable working in a clinical research environment, following study protocols, and maintaining clear, timely documentation. This is a per diem PRN position, with hours varying based on clinical and study needs. Pay is $45–$55 per hour, commensurate with experience.

Requirements

Current and unrestricted license to practice as a Registered Nurse in Pennsylvania.
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 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 as needed and in accordance with study protocols and nursing scope of practice.
Perform phlebotomy and assist with difficult blood draws.
Assist with collection of 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 collection and documentation of adverse events, concomitant medications, and medical history.
Assist with identification, documentation, and reporting of 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 in a timely manner 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.