About the Job

We are seeking a Clinical Research Coordinator (Research Professional 2) in the Department of Psychiatry & Behavioral Sciences. The primary purpose of this position includes: conducting assessments with research participants following IRB-approved protocols within the Minnesota Discovery Team in Addition (MDTA). Study visits for ongoing studies include but are not limited to: schedule, coordinate and administer structured clinical interviews, neurocognitive testing, MRI imaging, and neuromodulation sessions (cognitive training, transcranial electrical stimulation or transcranial magnetic stimulation). This position will assist with training of research assistant staff, team meetings, and maintaining meeting notes.

Job Duties/Responsibilities:

60% - Follow MDTA PI instructions on maintaining and running addiction research studies including: Advertise/Recruit participants from addiction treatment programs, Screening potential participants and with PI’s feedback determine eligibility, Consenting participants, Administering and supervise administration of MRI and neuromodulation sessions, Conduct follow-up visits with participants, Conduct cognitive assessments, Conduct structured clinical interviews, neurocognitive testing
10% - Assist with research staff training, meetings, checking in, tasks, and schedules
10% - Assist with data entry/management within RedCap/Qualtrics for multiple studies and verifying/ensuring complete data collection.
10% - Assist with maintaining regulatory binders including DOA, protocol training, notes to file for regulatory and each study binder.
10% - Assist with preparations for study monitoring.

Qualifications

Required Qualifications: BA/BS degree, plus at least two years of relevant experience, or a combination of education and relevant experience to equal at least six years. Willingness to visit addiction treatment center sites on a daily basis. Ability to demonstrate outstanding communication, organization, and interpersonal skills. Experience administering clinical (e.g. SCID) interviews. Experience with consenting following IRB standards. Ability to assist investigators with statistical analyses and interpretation of study data for grant applications by providing clean and complete data sets. Ability to coordinate participant transportation to the brain imaging centers for MRI scanning. Ability to foster strong relationships with study subjects and with the staff at partner treatment center sites. Participate in weekly team meetings and monthly coordinator meetings. Facilitate monthly meetings with research staff

Preferred Qualifications: Experience with TMS, tES, or EEG. Experience with cognitive training administration. Experience with MRI data collection and task fMRI administration. Experience with administering cognitive assessments. Clinical Research Coordinator Certification (CCRC). Extensive experience working with human subjects. Knowledge of neuroscience research

About the Job

Job Duties/Responsibilities:

60% - Follow MDTA PI instructions on maintaining and running addiction research studies including: Advertise/Recruit participants from addiction treatment programs, Screening potential participants and with PI’s feedback determine eligibility, Consenting participants, Administering and supervise administration of MRI and neuromodulation sessions, Conduct follow-up visits with participants, Conduct cognitive assessments, Conduct structured clinical interviews, neurocognitive testing
10% - Assist with research staff training, meetings, checking in, tasks, and schedules
10% - Assist with data entry/management within RedCap/Qualtrics for multiple studies and verifying/ensuring complete data collection.
10% - Assist with maintaining regulatory binders including DOA, protocol training, notes to file for regulatory and each study binder.
10% - Assist with preparations for study monitoring.

Qualifications

About the Job

Job Duties/Responsibilities:

60% - Follow MDTA PI instructions on maintaining and running addiction research studies including: Advertise/Recruit participants from addiction treatment programs, Screening potential participants and with PI’s feedback determine eligibility, Consenting participants, Administering and supervise administration of MRI and neuromodulation sessions, Conduct follow-up visits with participants, Conduct cognitive assessments, Conduct structured clinical interviews, neurocognitive testing
10% - Assist with research staff training, meetings, checking in, tasks, and schedules
10% - Assist with data entry/management within RedCap/Qualtrics for multiple studies and verifying/ensuring complete data collection.
10% - Assist with maintaining regulatory binders including DOA, protocol training, notes to file for regulatory and each study binder.
10% - Assist with preparations for study monitoring.

Qualifications

About the Job

Job Duties/Responsibilities:

60% - Follow MDTA PI instructions on maintaining and running addiction research studies including: Advertise/Recruit participants from addiction treatment programs, Screening potential participants and with PI’s feedback determine eligibility, Consenting participants, Administering and supervise administration of MRI and neuromodulation sessions, Conduct follow-up visits with participants, Conduct cognitive assessments, Conduct structured clinical interviews, neurocognitive testing
10% - Assist with research staff training, meetings, checking in, tasks, and schedules
10% - Assist with data entry/management within RedCap/Qualtrics for multiple studies and verifying/ensuring complete data collection.
10% - Assist with maintaining regulatory binders including DOA, protocol training, notes to file for regulatory and each study binder.
10% - Assist with preparations for study monitoring.

Study Coordinator - Research Professional 2

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Twin Cities, Minnesota, United States