Research Assistant - Brunswick, OH

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. Research Assistant Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies.

Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. We are seeking a full-time, on-site Research Assistant (RA).

The RA is a specialized research professional working with and under the direction of the Clinical Principal Investigator (PI) and site management. The primary responsibility of the RA is to assist the Clinical Research Coordinators with conduct of research studies. The RA supports and facilitates the daily clinical trial activities and plays a supportive role in the conduct of the study.

Responsibilities

Assists Study Team with communicating study

Requirements

to all individuals involved in the study Works with the Study Team to develop and implement recruitment strategies in accordance with site policies and IRB

and approvals Assists Study Team with screening subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion Assists Study Team as requested to register participants in the Clinical Trial Management System to ensure billing of study procedures to appropriate funding source Maintains inventory of study supplies.

and site policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms Aids the Study Team in maintaining effective and ongoing communication with sponsor, research participants, site management and PI during the course of the study Works with the Study Team to manage the day to day activities of the study including problem solving, communication and protocol management Collects and reports ongoing patient recruitment/ enrollment progress and metrics to site management and PI As directed, process and ship specimens per study protocol and IATA regulations Arranges secure storage of study documents that will be maintained according to Good Clinical Practice guidelines or for the contracted length of time, whichever is longer Enter all patient visit data in e-CRF and CTMS on a daily basis or as directed Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance Other duties as assigned Iterati