Research Nurse - Per Diem
About The Position
Adams Clinical is seeking a PRN Registered Nurse to provide flexible, as-needed on-site clinical support at its clinical research site in Philadelphia. The nurse 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, Good Clinical Practice (GCP) guidelines, and applicable research requirements. The role includes clinical tasks such as injections, investigational product preparation, IV catheterization and drug infusion, phlebotomy, medical record and clinical results review, medication reconciliation, and medical liaison activities. The nurse follows study protocols and maintains clear, accurate, and timely documentation to support participant safety and compliant study conduct. Hours vary according to clinical and study needs.
Requirements
- Current, unrestricted Registered Nurse license 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 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 IV catheters 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 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 patient-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; assist 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.
Benefits
- 401(k) matching
- Medical, dental, and vision insurance
- Employee assistance program
- Flexible spending account
- Health savings account
- Life insurance
- Paid time off
- Parental leave
- Professional development assistance
