Research Assistant - Brunswick, OH

Research Assistant

We are seeking a full‑time, on‑site Research Assistant (RA) at Iterative Health. The RA works under the direction of the Clinical Principal Investigator (PI) and site management, supporting the Clinical Research Coordinators in the conduct of research studies. The primary responsibility of the RA is to assist with daily clinical trial activities and play a supportive role throughout the study.

• Assist the Study Team with communicating study requirements to all individuals involved.
• Help develop and implement recruitment strategies in accordance with site policies and IRB requirements.
• Screen subjects for eligibility using protocol‑specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.
• Register participants in the Clinical Trial Management System to ensure billing of study procedures to the appropriate funding source.
• Maintain inventory of study supplies; if handling investigational drugs/devices, follow sponsor protocol and/or site policies on accountability.
• Assist in completing study documentation and maintenance of study files in accordance with sponsor requirements and site policies, including consent forms, source documentation, narrative notes, case report forms, and investigational material accountability forms.
• Help maintain effective and ongoing communication with the sponsor, research participants, site management, and PI during the study.
• Work with the Study Team to manage day‑to‑day activities of the study, including problem solving, communication, and protocol management.
• Collect and report ongoing patient recruitment/enrollment progress and metrics to site management and PI.
• Process and ship specimens per study protocol and IATA regulations as directed.
• Arrange secure storage of study documents to 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.
• Assist in protecting 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 non‑compliance.
• Other duties as assigned.

• 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.

• High school diploma or equivalent; some college preferred.
• Minimum 2 years in a healthcare setting.
• 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 hiring process. If you require any accommodations to make the application process or interview experience more accessible, please contact Candidate Accommodationslth.