Research Intern - Cedar Park, TX

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 Intern. The Intern 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 Intern is to assist the Clinical Research Coordinators with conduct of research studies. The Intern supports and facilitates the daily clinical trial activities and plays a supportive role in the conduct of the study, especially related to patient eligibility and recruitment.

Responsibilities

Assist clinical research staff with reviewing protocols for patient eligibility criteria; Assist with managing recruitment and referral networks, screening subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion and prioritizing patients for outreach and follow up; Learn to navigate various databases and referral sources for patients, including the Electronic Medical Record (EMR) and other clinical databases; Document patient information in the Clinical Trials Management System; Work with the Study Team to develop and implement recruitment strategies in accordance with site policies and IRB requirements and approvals; Under guidance from research staff, become proficient in navigating research, study protocols, and chart reviews to complete the above tasks; Assist Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations; Cooperate with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance; Other duties as assigned

Requirements

High school diploma or equivalent; Strong written and verbal communication skills; Ability to read, interpret, and apply clinic policies and research protocols; Ability to use standard office software; Must be able to lift up to 25 pounds

Nice to have

Some college preferred