Outcomes Specialist I, CHeT

Supports research projects focused on the development, validation, and analysis of patient-reported (PRO) outcome measures in academic research and Contract Research Organization environments. Assists with the collection and tracking of research documentation, the coordination of study files, and operational support for PRO development activities. Participates in outward-facing communications, external sponsor interactions, and relationship-building with industry collaborators to support project operations and increase organizational visibility.

Responsibilities

Coordinates and implements research studies from protocol preparation and IRB submission through study execution; Manages participant recruitment, conducts patient and caregiver interviews, develops and programs REDCap study instruments, deploys electronic surveys, and oversees data collection activities; Monitors study progress and data quality to ensure compliance with approved protocols, regulatory requirements, and study timelines; Analyzes and interprets quantitative and qualitative data to develop and validate patient- and caregiver-reported outcome measures; Identifies relevant grant opportunities and develops supporting materials for grant applications and research funding proposals; Prepares abstracts, presentations, and manuscripts to disseminate research findings; Performs additional research-related responsibilities; Other duties as assigned

Requirements

Bachelor’s Degree in a relevant field such as Public Health, Clinical Research, Health Sciences, Psychology, Neuroscience, or a related discipline and 1 year of experience in clinical research coordination, outcomes research, technology-based research, or a related research environment; Or equivalent combination of education and experience; Ability to analyze and interpret basic statistical and research data; Familiarity with survey-based research methodologies and patient-reported outcomes research; Proficiency in Microsoft Word, Excel, and PowerPoint; Strong attention to detail and organizational skills; Excellent written and verbal communication skills

Nice to have

Experience working with human subject research protocols, REDCap, survey development, or patient-reported outcome measures; Ability to coordinate multiple research activities and manage competing priorities; Strong interpersonal skills for engaging with patients, collaborators, and research sponsors