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Research Assistant (Research Pro 1)
University of Minnesota, Twin Cities
This entry level study coordinator position will support the EPINET project within the Vinogradov Lab. This project is part of a national NIMH initiative which aims to create a network of early psychosis intervention treatment centers offering specialty care to individuals with a recent onset psychotic illness. This study has two primary components. In the first, we are examining longitudinal measurement based care, comprised of self-report assessments and remote interviews conducted through teleconferencing applications; the data from these assessments will generate a personalized report which will be presented to the participant by a clinical team member. The second component is a 12-week mobile intervention of cognitive training and motivational enhancement using mobile applications, which the participant will complete at home. This project will be a multi-site study with four recruiting locations: Fairview Riverside, HCMC, Saint Louis Park, and Duluth. The incumbent of this position will be the primary study coordinator for the Fairview Riverside location, but may also be required to support additional protocols within the lab. The incumbent must be able to work independently and have excellent organizational and interpersonal skills. This role will have hybrid duties. The incumbent will spend a significant portion of their time interfacing with the clinical care team, and will support measurement based care activities in the role of a Psychometrist. In this capacity, the incumbent will be responsible for scheduling appointments with adolescent and adult patients in the First Episode Psychosis clinics, conducting patient interviews, supervising self-report patient measures, and facilitating ancillary measurement based care activities. The incumbent will receive training for conducting diagnostic and clinical assessments of psychotic symptoms and neurocognitive functioning, as needed. In addition, this role will have significant duties related to research activities. In this capacity, the incumbent will be responsible for the recruitment of adult and adolescent participants, scheduling and conducting study appointments, data management tasks, and regulatory documentation. The incumbent will receive training in GCP and federal regulations surrounding clinical research, data safety practices, assessing capacity to consent and conducting informed consent, and regulatory management and documentation. Training for specialized equipment will be provided as needed. Data Collection (50%): Database and Regulatory Management (20%): Participant Recruitment and Retention (20%): Lab support tasks (10%):
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All required qualifications must be documented on application materials Required Qualifications:
Preferred Qualifications:
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Clinical Research Coordinator (Research Pro 1) | Minneapolis, Minnesota |
University of Minnesota, Twin Cities | 1 Month Ago |
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