Research Intern - Cedar Park, TX

Iterative Health; Cedar Park (TX); On-site; USD 36,000 - 48,000; Full time

Job summary

Iterative Health in Cedar Park, Texas, is seeking a full-time, on-site Research Intern to support Clinical Research Coordinators in daily trial activities. You will help assess patient eligibility, screen potential participants, and manage recruitment networks within protocol and IRB requirements.

You will document patient data in the CTMS, assist with recruitment strategies, and learn to navigate EMR and study protocols under supervision.

Qualifications

• 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.

Responsibilities

• Assist clinical research staff with reviewing protocols for patient eligibility criteria
• Assist with managing recruitment and referral networks, screening subjects for eligibility using inclusion/exclusion criteria
• Learn to navigate EMR and other clinical databases
• Document patient information in the Clinical Trials Management System
• Develop and implement recruitment strategies in line with IRB approvals
• Under guidance, navigate study protocols and chart reviews to complete tasks
• Protect the rights and welfare of human research participants per regulations
• Cooperate with site compliance and PHI access/disclosure controls
• Other duties as assigned

Skills

Strong written and verbal comms

Policy/protocol interpretation

Office software proficiency

Lifts up to 25 pounds

Education

High school diploma or equivalent

Some college preferred

Job description

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 Intern

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
• Works 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
• 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

All employees are expected to:

• Perform quality work within deadlines with or without direct supervision
• Interact professionally with other employees, customers and suppliers
• Work effectively as a team contributor on all assignments
• Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations

Qualifications

• High school diploma or equivalent. Some college preferred
• 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

At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.

At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact [e-mail].