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Research Scientist, Level 1 Jobs
Company | University of Colorado Boulder |
Address | Boulder, CO, United States |
Employment type | FULL_TIME |
Salary | |
Category | Higher Education |
Expires | 2023-07-17 |
Posted at | 11 months ago |
Job Summary
- The postdoctoral research associate will work closely with the PI to assure data quality control and the assurance of data safety and monitoring and in this role will assist the PI to conduct quarterly meetings with the external Data Safety and Monitoring Board. Support for grant writing, data management and analysis, manuscript preparation, and annual NIH progress reporting will also be expected.
- We seek a full-time Postdoctoral Research Associate to aid with NIH-funded ERP studies of acute influences of THC and CBD on memory encoding and retrieval processes.
- Primary responsibilities include the supervision, design, implementation, analysis, and publication of EEG data.
- The postdoctoral research associate will be responsible for coordinating with the Pl and investigative team in order to manage the collection of behavioral and biological data, correspondence with the IRB regarding updates and amendments to relevant protocols, and supervision and training of research staff.
- Specifically, it is expected that the postdoctoral research associate will take a lead role in mentoring undergraduates, professional research assistants, and graduate students, analyzing data, preparing data for presentation at professional conferences, and will collaborate with the PI and Co-Investigators to submit manuscripts for publication.
- Ph.D. in psychology, cognitive science, neuroscience, or another related field.
- EEG/ERP experience (preferably with EGI systems).
- Ability to work collaboratively with study staff, postdoctoral researchers, undergraduates, principal investigators, and other laboratories.
- Experience with computer programming, computer networking, and Matlab.
- Research experience in cognitive psychology or related areas.
- Experience conducting human participant research appointments and eligibility screenings.
- Strong communication and organizational skills.
- REDCap project design and management.
- Experience conducting human clinical trials research and complying with IRB guidelines.
- Literacy in R/RStudio, SPSS, statistical analyses.
- Resume or CV.
- Cover letter addressed to the Search Committee briefly describing your qualifications, professional goals, and specific interest in this position.
- A PDF Sample of Work.
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