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Research Study Coordinator -Psychometry (Contract / Part-Time)

Company

BrainCheck

Address Austin, TX, United States
Employment type CONTRACTOR
Salary
Category Internet Publishing
Expires 2023-07-01
Posted at 11 months ago
Job Description
Founded in 2015 by neuroscientists and technologists Drs. Yael Katz and David Eagleman, BrainCheck helps reduce the human and economic toll of cognitive impairment and dementia through its interactive cognitive assessment and care management technology. We are used in over 500 primary care and neurology practices as well as several brand-name health systems and payers including UPMC, Advocate Aurora, and Humana.


We are looking for a part-time Research Study Coordinator to run and facilitate data collection for one of our active research studies. Daily work will be predominantly on-site with limited remote work.


This role will lead initiatives for the specified research study around the greater Austin area. The majority of your time will be spent recruiting, enrolling, obtaining consent, conducting study sessions, and inputting data within an electronic system. It is expected that you will be self-directed and a champion at working independently. This role is expected to entail around 20 - 30 hours per week. You must be comfortable working with an older population and proactive in helping them navigate the challenges of research participation. We are looking for you to bring your creativity to problem-solving and help meet our ambitious goals.


Duties and Functions


  • Assist in general research study etiquette ensuring adherence to protocol, GCP, HIPAA, and regulatory requirements
  • Conduct study procedures with participants including administering neuropsychologist tests, collecting informed consent, and completing questionnaires
  • Coordinate the collection and organization of materials and data used for the study
  • Capture, input, and clean study data using an electronic data capture system
  • Perform other related duties incidental to the work described herein
  • May assist with compiling and maintaining quality and regulatory study-related documents and IRB duties as needed
  • May collaborate with the primary investigator, sponsor, and research staff to plan, conduct and evaluate project protocols and activities
  • Lead and coordinate recruitment and scheduling of participants


Qualifications


  • This position will require you to be fully vaccinated based on the latest CDC protocol
  • Education/Experience: - Education, coursework, or degree in a related discipline, or equivalent combination of education and experience
  • Experience conducting human subjects research, data collection, and working with individuals in a professional setting


Qualities


  • Being able to quickly troubleshoot and resolve arising issues or circumstances as they come
  • Must be self-directed with demonstrated ability to work independently Ability to withstand extended periods of sitting
  • Great communicator with the ability to understand a concept and convey it clearly and concisely
  • Detail-oriented multitasker with exceptional organization and the ability to effectively manage yourself
  • Open to potentially working irregular hours including weekends


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