Research Assistant - Flowood, MS

Minimum 2 years in a healthcare setting

Ability to read, interpret, and apply clinic policies and research protocols

At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves.

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 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 forms, and investigational material accountability forms