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Research Associate - Department Of Psychiatry - Hoth Lab
Company | University of Iowa |
Address | Iowa City, IA, United States |
Employment type | FULL_TIME |
Salary | |
Category | Higher Education |
Expires | 2023-06-12 |
Posted at | 1 year ago |
The Department of Psychiatry at the University of Iowa is seeking a Research Associate to join Dr. Karin Hoth’s research team to study factors that impact cognitive functioning and symptoms of depression and anxiety among individuals with chronic cardiopulmonary medical conditions (e.g., COPD, sarcoidosis). The Research Associate will support clinical research by managing and analyzing data (including neuropsychological, physiological and neuroimaging measures), recruiting and scheduling participants, administering cognitive tests and questionnaires, managing regulatory paperwork, and working with investigators, staff and students as a member of an interdisciplinary team.
- Oversee data management for NIH-funded studies and utilize statistical software to assist in the preparation of material for inclusion in reports, publications and presentations.
- Perform library research on specified topics and prepare bibliographies and abstracts according to instructions. Assist in the preparation of materials for scientific reports to be written by faculty on the research project, including scientific abstracts, poster presentations, and peer-review manuscripts.
- Schedule and facilitate collection of physiological study measures and MRI reservations in conjunction with medical and nursing staff.
- Occasionally travel off-campus to other medical and community centers to conduct research/recruitment and to meet with investigators, researchers, and potential participants.
- Create, maintain, and audit databases for projects, including identification and correction of discrepancies, assigning appropriate access privileges to research staff, adding new or updated measures, and compiling requested data sets for analysis.
- Perform other duties as assigned.
- Score and record new data collected; oversee data entry and data auditing.
- Manage, prepare, and organize regulatory documentation. Communicate with IRB staff, investigators, funding agencies, and regulatory authorities. Monitor compliance to regulatory guidelines and proper maintenance of documents. Ensure regulatory reports and reviews are submitted on time.
- Administer cognitive tests and questionnaires with careful attention to detail.
- Participate actively in lab meetings and be prepared to present progress reports on coordination issues to be addressed and any issues requiring investigators’ attention.
- Oversee participant recruitment efforts. This includes recruiting and interviewing prospective participants for studies, obtaining informed consent, detailing medical/neurological history, completing questionnaires and reviewing data with investigators.
- Demonstrate strong communication skills via telephone including rapidly developing rapport with potential research participants and speaking clearly and effectively over the phone.
- Assist in the design, development, execution, administration and maintenance of new protocols and clinical research studies.
- Review compliance with protocol, organize and maintain study materials and files in conjunction with other research staff.
- Develop and maintain positive working relationships with the research team including neuropsychologists, internal medicine physicians, physiologists, radiologists, students and research support personnel.
- Schedule: Full-time
- Appointment Type: Professional and Scientific
- Classification Title: Research Associate
- Pay Level: 4A
- Contact Name: Lori Posey
- Organization: Healthcare
- Contact Email: [email protected]
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