Research Assistant

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.Research AssistantIterative 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 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.ResponsibilitiesAssists Study Team with communicating study requirements to all individuals involved in the studyWorks with the Study Team to develop and implement recruitment strategies in accordance with site policies and IRB requirements and approvalsAssists Study Team with screening subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant's eligibility or exclusionAssists Study Team as requested to register participants in the Clinical Trial Management System to ensure billing of study procedures to appropriate funding sourceMaintains inventory of study supplies. If handling investigational drugs/devices, follows the sponsor protocol and/or site policies on Investigational Drug/Device AccountabilityAssists 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 formsAids the Study Team in maintaining effective and ongoing communication with sponsor, research participants, site management and PI during the course of the studyWorks with the Study Team to manage the day to day activities of the study including problem solving, communication and protocol managementCollects and reports ongoing patient recruitment/ enrollment progress and metrics to site management and PIAs directed, process and ship specimens per study protocol and IATA regulationsArranges secure storage of study documents that will be maintained according to Good Clinical Practice guidelines or for the contracted length of time, whichever is longerEnter all patient visit data in e-CRF and CTMS on a daily basis or as directedAssists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulationsCooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncomplianceOther duties as assignedIterative Health ExpectationsAll employees are expected to: Perform quality work within deadlines with or without direct supervisionInteract professionally with other employees, customers and suppliersWork effectively as a team contributor on all assignmentsWork independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizationsQualifications High school diploma or equivalent. Some college preferredMinimum 2 years in a healthcare settingStrong written and verbal communication skilsAbility to read, interpret, and apply clinic policies and research protocolsAbility to use standard office softwareMust be able to lift up to 25 poundsAt 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.health.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.health.