Nurse Practioner​/Physician Assistant

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.

Adams Clinical is seeking a PRN Nurse Practitioner (NP) or Physician Assistant (PA) to provide flexible, as‑needed clinical support across our New York City area research sites (10029 and 10461). This role works under the supervision of our physician Principal Investigators and Clinical Operations leadership on the conduct of pharmaceutical‑sponsored clinical trials in accordance with FDA regulations and GCP guidelines.

Typical tasks will include, but are not limited to, IV catheterization and drug infusion, injections, phlebotomy, medical record and clinical results review, medication reconciliation, and medical liaising. The ideal candidate will have recent injection experience and 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.

• Availability to provide on‑site clinical support at least 2 weekdays per week, as needed to support protocol‑required activities and participant visits. The expected frequency of availability may be adjusted based on applicable study protocols, site needs, and operational requirements
• IV placement, initiation and monitoring of IV infusions in accordance with the study protocol
• Administer subcutaneous and intramuscular injections in accordance with study protocols
• Perform physical exams and other protocol‑required assessments within scope of practice
• Perform clinical review and assessment of protocol‑required results and clinical data (e.g., laboratory results, ECGs, and vital signs) in collaboration with site Principal Investigators
• Identify and elevate 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
• Assist with difficult phlebotomy and IV placement for blood collection, as needed
• Review medical records and reconcile relevant information with patient‑reported history
• Assist with collection and documentation of adverse events (AEs), concomitant medications, medical history
• Assist with identification, documentation, and reporting of Serious Adverse Events (SAEs), including required regulatory/IRB documentation
• Provide on‑site clinical support during emergency situations, as needed
• Document clinical assessments, procedures, and participant‑related information accurately and in a timely manner in accordance with study protocols and applicable requirements
• Provide PRN clinical support across both New York City research sites, with willingness and ability to commute between locations as needed

• Bachel…