Research Assistant - New Albany, IN
About The Position
Iterative Health is a healthcare technology and services company focused on accelerating 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. The company focuses on driving the success and growth of partner sites by empowering them with tech-enabled services, combining deep expertise in clinical trials with cutting-edge AI to expand and expedite access to novel therapeutics for patients. The company is seeking a full-time, on-site Research Assistant (RA) who will work 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 the conduct of research studies, supporting and facilitating daily clinical trial activities and playing a supportive role in the conduct of the study.
Requirements
- High school diploma or equivalent
- Minimum 2 years in a healthcare setting
- Strong written and verbal communication skils
- 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 Haves
- Some college preferred
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 forms, and investigational material accountability forms
- Aids the Study Team in maintaining effective and ongoing communication with sponsor, research participants, site management and PI during the course of the study
- Works with the Study Team to manage the day to day activities of the study including problem solving, communication and protocol management
- Collects and reports ongoing patient recruitment/ enrollment progress and metrics to site management and PI
- As directed, process and ship specimens per study protocol and IATA regulations
- Arranges secure storage of study documents that will 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
- Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations
- Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance
- Other duties as assigned
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
