Redcap Data Analyst Jobs in Iowa (NOW HIRING)

The Department of Psychiatry at the University of Iowa is seeking a Research Assistant.  This position is within the laboratories of Dr. Nicholas Trapp and Dr. Aaron Boes whose lab's current projects aim to better understand the neuroanatomical and circuit-based pathophysiology of neuropsychiatric disorders, with an emphasis on the development and optimization of stimulation-based neurotherapeutics.  Research methods include structural and functional neuroimaging, electrophysiology, and clinical trial design.

The Research Assistant will be responsible for coordinating day-to-day clinical research activities by assisting, preparing and submitting the appropriate Human Subjects Review forms and application materials to the Institutional Review Board, assisting with subject recruitment, scheduling, retention, and enrollment; preparing and overseeing data entry; maintaining routine compliance with regulatory agencies; training and assisting new lab members with their projects.

Characteristic Duties and Responsibilities
    Exhibit satisfactory knowledge of research techniques and procedures relating to the performance of clinical research, especially those related to neuropsychiatric disorders and neuromodulation techniques including transcranial magnetic stimulation (TMS) and frameless neuronavigation. 
    Display excellent interpersonal sensitivity and communication skills by developing and maintaining a positive working relationship within an interdisciplinary research team.
    Demonstrate excellent organizational skills and documentation in a research setting.
    Assist in the preparation of regulatory submissions and updating documents to necessary agencies.
    Collaborate with Principal Investigators and the study team in the development, execution, administration and maintenance of protocols and clinical studies.  As skills develop, provide input into descriptions of complex research procedures.
    Responsible for scheduling participants for procedures or follow up as required by the study protocol or design, arrange for follow-ups with study participants and maintain records of their visits and interviews. 
    Update and maintain lab manuals for onboarding and training lab members.
    Obtain informed consent and other required regulatory documents and monitor participant experience for reportable events. 
    Participate in the collection, and entry of data into clinical trial research data systems.
    Perform data management and analysis with standard software.
    As skills develop, coordinate with staff or students engaged in data collection to provide instruction on techniques, as well as consultation on project work.
    Assist with the preparation and submission of documents related to research protocol annual reviews, modifications, Adverse Events, Safety Reports and other reportable events to IRB, as needed.
    May be called upon to interview and train new staff on clinical trial and testing procedures and supervise implementation of research protocols. May supervise and/or facilitate the progress of students working on research projects.

Staff Type: Professional and Scientific
Pay Level: 3A
Type of Position: Full-time, Specified Term, 12 months with possibility of extension