Jobs · Healthcare · Pennsylvania

NP/PA — BOTOX® Injector - Philadelphia

Adams Clinical · Philadelphia, PA · 1 mo ago
On-siteHealthcare$75–$87/hrFull-time

About the role

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.

Responsibilities

  • Provide on‑site clinical support at least 2 weekdays per week as needed to support protocol‑required activities and participant visits (frequency adjustable per study protocol, site needs, and operational requirements).
  • Perform IV catheterization, initiation, and monitoring of IV infusions in accordance with the study protocol.
  • Administer subcutaneous and intramuscular injections per study protocol.
  • Support preparation and handling of investigational product as permitted by the protocol, site procedures, and applicable requirements.
  • Perform physical exams and other protocol‑required assessments within scope of practice.
  • Review and assess protocol‑required clinical data (laboratory results, ECGs, vital signs) in collaboration with site Principal Investigators.
  • Identify and escalate clinically significant findings, changes in participant condition, and potential reactions to study dosing that may impact participant safety or subsequent dosing, in collaboration with Principal Investigators.
  • 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, and medical history.

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