Clinical Research Nurse (PRN)

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

As a member of our clinical team, you will work under the supervision of our physician principal investigators and clinical nurse manager on the conduct of pharmaceutical-sponsored clinical trials in accordance with FDA regulations and GCP guidelines. Typical tasks will include but not be limited to IV catheterization and drug infusion, injections, phlebotomy, medical record and lab results review, reconciling medications, and medical liaising. The ideal candidate will have recent bedside experience. Clinical research experience is a plus. In addition, clinical research nurses at Adams Clinical will also work closely with other members of the study team, providing mentoring, direction, and guidance to clinical research coordinators. This position will also involve general research-related responsibilities like facilitating the informed consent process, administration of screening procedures, data entry, maintenance of regulatory binders, and other nursing functions as required in support of the clinical trial.

Key Responsibilities:

• IV placement, initiation and management of IV infusions per sponsor provided protocol

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