Research Assistant - Wichita, KS

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.

We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.

The Research Assistant (RA) at Iterative Health is an essential on-site member of the clinical research team, working under the direction of the Principal Investigator and site management to support the day-to-day conduct of active clinical trials.

This role assists Clinical Research Coordinators across every phase of study execution from participant screening and enrollment through documentation, data entry, and compliance. The ideal candidate is a detail-oriented, team-first professional with a healthcare background and a genuine interest in advancing clinical research. This role is a strong entry point into the clinical research field with real exposure to the full study lifecycle.

Where You’ll Drive Impact

• Assist the Study Team with communicating study requirements to all individuals involved in the study.

• Work with the Study Team to develop and implement recruitment strategies in accordance with site policies and IRB requirements.

• Assist with screening subjects for eligibility using protocol-specific inclusion and exclusion criteria, documenting each potential participant's eligibility or exclusion.

• Assist with registering participants in the Clinical Trial Management System (CTMS) to ensure proper billing of study procedures to the appropriate funding source.

• Collect and report ongoing patient recruitment and enrollment progress and metrics to site management and the PI.

• Assist the Study Team in completing study documentation and maintaining study files in accordance with sponsor requirements and site policies, including consent forms, source documentation, case report forms, and investigational material accountability forms.

• Enter all patient visit data in eCRF and CTMS on a daily basis or as directed.

• Arrange secure storage of study documents in accordance with GCP guidelines or the contracted length of time, whichever is longer.

• Maintain inventory of study supplies; follow sponsor protocol and site policies on investigational drug/device accountability when applicable.

• Process and ship specimens per study protocol and IATA regulations as directed.

• Work with the Study Team to manage the day-to-day activities of the study, including problem-solving, communication, and protocol management.

• Aid the Study Team in maintaining effective and ongoing communication with sponsors, research participants, site management, and the PI throughout the course of each study.

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