Research Intern Providence, RI

mbining 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.
Research

Intern

We are seeking a full‑time, on‑site Research Intern. The Intern is a specialized research professional working under the direction of the Clinical Principal Investigator (PI) and site management. The primary responsibility is to assist the Clinical Research Coordinators with the conduct of research studies, supporting daily clinical trial activities and playing a supportive role in 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 in accordance with federal regulations.
• Cooperate with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and report instances of noncompliance.
• Perform 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 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.
Equal Employment Opportunity

As set forth in Iterative Health’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.

At Iterative Health, we’re actively working toward creating an environment that is representative of the diversity of patients our technology serves. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact Candidate Accommodationslth.
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