Paramedic - PRN

Note: The internal title for a licensed paramedic at ICON is Senior Research Associate. Further details below.

ICON plc is a world-leading clinical research organization. We advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.

With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

The Role:

Our full-service clinic in Lenexa, Kansas, is a 114-bed, state-of-the-art research center, located near metropolitan Kansas City.

We are seeking a (PRN) Senior Medical Research Associate with active Paramedic licensure to support clinical research studies at our Lenexa, Kansas (KS) clinic.

Whether you’re exploring a career in clinical research or already have experience in the field, this role offers a chance to contribute to work that supports the future of healthcare and disease management. Paramedic candidates without research experience are encouraged to apply.

Key Responsibilities

The Senior Medical Research Associate opportunity blends patient care with research responsibilities.

Clinical & Paramedic Responsibilities

• Provide direct patient care within the onsite clinic, including advanced assessment, triage, vital signs, and urgent clinical support.

• Perform Paramedic‑level procedures within licensure scope, including IV placement, blood draws, specimen collection, injections, wound care, and emergency response/stabilization.

• Monitor participant safety during research procedures and respond promptly to medical concerns, adverse events, or unexpected clinical situations.

• Ensure medical equipment, supplies, and emergency materials are maintained, stocked, and fully operational.

Research & Operational Responsibilities

• Assist in planning, coordinating, and executing clinical research activities in alignment with study protocols and regulatory requirements.

• Support study visit procedures, including sample handling, documentation, timing, and protocol‑driven tasks.

• Conduct or support staff training, reinforce protocol adherence, and provide ongoing operational assistance to investigators and team members.

• Track study progress, maintain accurate and audit‑ready documentation, and ensure high‑quality records throughout the study lifecycle.

• Contribute to the development and review of study materials, including source documents, manuals, logs, and operational tools.

Qualifications

• Active, unrestricted Paramedic state license.

• National Registry Paramedic (NRP) certification or state‑recognized equivalent.

• Strong understanding of patient assessment, emergency response protocols, and clinical documentation standards.