Clinical Research Coordinator
- Recruited, screened, and obtained informed consent from new study participants- Scheduled, organized, tracked, and oversaw study assessments and procedures- Administered functional MRI tasks- Conducted recorded open-ended interviews with study participants with schizophrenia or at clinical high risk for psychosis- Conducted semi-structured clinical interviews with study participants to assess symptom severity, mood, and social/role functioning- Cleaned and curated study data and prepared data for analysis, including: - Constructing and maintaining REDCap forms for holding study data - De-identifying MRI data and organizing into the Brain Indices Data Structure - Organizing data for NIMH Data Archive submissions - Writing a Python script to perform named entity recognition on transcripts of study participant interviews to assist with de-identification - Setting up WhisperX audio-to-text transcription and diarization pipeline- Stored and shipped frozen biological samples- Interviewed, hired, and trained new lab members- Mentored undergraduate volunteers and provided support with career development- Led a weekly tutorial session on data analysis in Python for coworkers- Authored study protocol and informed consent forms for a new R01 study- Corresponded with the ISMMS Institutional Review Board regarding study modifications and regulatory compliance- Prepared budgets and gathered documents for review by the ISMMS Grants and Contracts Office for grant applications, new awards, and research progress reports- Assisted with qualitative thematic analyses of open-ended interviews conducted with study participants- Analyzed transcripts of open-ended interviews with individuals with schizophrenia or at clinical high risk for psychosis to examine lexical diversity and etymology of words used