CHeT Outcomes Research Coordinator
General Purpose:
Plans, coordinates and conducts/implements all research activities associated with the development of patient and caregiver reported outcome measures, longitudinal studies and instrument translations/cultural validations. These responsibilities include interaction with study sponsor, recruitment partners, and patients. Interprets research data at the completion of each phase of instrument development and at completion of study milestones creates written summaries with tables and figures for distribution to study sponsors and for presentation at various industry events.
Specific Responsibilities:
Under general direction within policy guidelines and approved protocols:
Under the direction of the Principal Investigator, assists in the conduct of research studies beginning with the preparation of IRB materials through the following activities, all within scope of approved protocol: coordinates subject recruitment, conducts patient interviews, programs data instrument in REDCap, implements REDCap surveys, monitors data collection within REDCap. (30%)
Conducts analysis and interpretation of collected data from research studies in anticipation of validating patient and caregiver reported outcome measures. (25%).
Researches grant opportunities and assists with preparation of grant application materials. Assists with the preparation of study proposals for potential collaborators. Prepares grant and study sponsor milestone reports. Presents data to grant-making organizations or study sponsors as requested. (20%)
Disseminates research findings by drafting abstracts, presentations, and publications for peer review and industry forums. Participates in professional associations/organizations dedicated to the neurologic diseases addressed in our research. Demonstrates accountability for continuous learning. Keeps current with industry standards, best practices, trends in therapeutic areas relevant to research studies; maintains team organizational practices. (20%)
Other duties and responsibilities as assigned. (5%)
Requirements:
· Bachelors’ Degree and 1- 2 years’ experience in clinical research coordination or technology research; or equivalent combination of education and experience.
· Ability to perform and analyze basic statistical information.
· Knowledge of =Microsoft Word, Excel and Powerpoint.
· Strong attention to detail and excellent interpersonal and communication skills, including writing ability.