Join Us in Shaping the Future of Clinical Research
Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core values— Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration —we create an environment where meaningful work drives meaningful change.
At Adams Clinical, you’ll find:
A culture of respect, transparency, and continuous improvement
Opportunities for professional growth and learning
A team dedicated to improving lives through innovation and integrity
If you’re passionate about making an impact in clinical research and want to be part of a collaborative, mission-driven organization, we’d love to have you on our team.
Job Role
Adams Clinical is seeking a PRN Nurse (RN) to provide flexible, as-needed on-site clinical support at our clinical research site located in The Bronx. This role works under the direction of physician Principal Investigators and Clinical Operations leadership in the conduct of pharmaceutical-sponsored clinical trials in accordance with study protocols, FDA regulations, GCP guidelines, and applicable research requirements.
Typical tasks will include, but are not limited to, injections, investigational product (IP) preparation, IV catheterization and drug infusion, phlebotomy, medical record and clinical results review, medication reconciliation, and medical liaising. The ideal candidate must be comfortable working in a clinical research environment, following study protocols, and maintaining clear and timely documentation in accordance with study protocols and applicable research and regulatory requirements.
Key Responsibilities:
Support the preparation and handling of investigational product (IP), as needed and as permitted by the study protocol, site procedures, and applicable requirements
Administer subcutaneous and intramuscular injections, as needed in accordance with study protocols and nursing scope of practice
IV placement, initiation and monitoring of IV infusions, as needed in accordance with the study protocol and nursing scope of practice
Perform phlebotomy and assist with difficult blood draws, as needed
Assist with collection of vital signs and other protocol-required clinical assessments, as needed
Identify and escalate clinically significant findings, changes in participant condition, and potential reactions to study dosing, including those that may impact participant safety or subsequent 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 (AEs), concomitant medications, and medical history
Assist with identification, documentation, and reporting of Serious Adverse Events (SAEs), including required regulatory/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 and medical sub-Investigators, Clinical Operations, Clinical Research Coordinators, and other study team members to support safe and efficient study conduct
Qualifications:
Current and unrestricted license to practice as a Registered Nurse in the state of New York required
Bachelor’s degree in nursing (BSN) required
2+ years of experience as a nurse preferred
Recent bedside…