Iterative Health
Healthcare
ResearchAssistant
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Research Assistant at Iterative Health. Skills: Clinical research, Patient screening, Data entry. Assist study team with communicating study requirements. Develop and implement recruitment strategies”
Industry & Context.
Problem solving
Lift up to 25 pounds
What They're Looking For.
Must Have
Minimum 2 years healthcare setting, 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
What You'll Do.
Assist study team with communicating study requirements
Develop and implement recruitment strategies
Screen subjects for eligibility
Register participants in CTMS
Maintain inventory of study supplies
Follow sponsor protocol on Investigational Drug/Device Accountability
Complete study documentation
Maintain effective communication with sponsor
Manage day to day activities of the study
Collect and report patient recruitment/enrollment progress
Process and ship specimens
Arrange secure storage of study documents
Enter patient visit data in e-CRF and CTMS
Assist in protection of rights and welfare of
Cooperate with site compliance and monitoring efforts
Report instances of noncompliance
Perform quality work within deadlines
Interact professionally with employees
customers and suppliers
Work effectively as a team contributor
How You'll Work.
Team & Collaboration
Assist Study Team; Work with Study Team; Work with site management and PI; Communicate with sponsor, research participants, site management and PI; Work with the Study Team to manage day to day activities; Communicate work efforts with other employees and organizations
Communication Scope
Written communication; Verbal communication
Full Job Description
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 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. 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 requirements 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. If handling investigational drugs/devices, follows the sponsor protocol and/or site policies on Investigational Drug/Device Accountability Assists Study Team in completing study documentation and maintenance of study files in accordance with sponsor requirements and site policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report
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