Research Associate - Trapp Lab - Psychiatry

University of Iowa•Iowa City, IA

17h•Onsite

About The Position

The Department of Psychiatry at the University of Iowa is seeking a Research Associate to join the laboratory of Dr. Nicholas Trapp. The Research Associate will be responsible for coordinating day-to-day clinical research activities by overseeing, preparing and submitting the appropriate Human Subjects Review forms and application materials to the Institutional Review Board, managing subject recruitment, scheduling, retention, and enrollment; preparing and overseeing data cleaning and management; maintaining routine compliance with regulatory agencies; working with study staff to draft papers for publication; training and assisting more junior lab members with their projects including compliance with protocols, data curation and analysis. The Trapp 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.

Requirements

Bachelor’s degree or an equivalent combination of education and experience.
Minimum 3 years of clinical research experience.
Experience with individuals with various neuropsychiatric disorders such as major depressive disorder, schizophrenia, bipolar disorder, substance use disorders, or epilepsy.
Prior experience performing Transcranial Magnetic Stimulation (TMS) on human subject participants.
Experience collecting various physiological measures such as electroencephalography (EEG), autonomic measures (galvanic skin response), and electrocardiograms (ECG).
Demonstrated ability to successfully multitask by effectively allocating time and managing involvement in several research projects.
Demonstrated ability to manage complex information with attention to detail and a high level of accuracy.
Excellent verbal, written, and interpersonal communication skills.

Nice To Haves

Advanced degree in psychology, neuroscience, or other health sciences.
Prior knowledge and experience with designing and implementing REDCap projects and Qualtrics surveys.
Baseline knowledge of statistical software, such as SPSS, RStudio or MATLAB.
Knowledge of University of Iowa policies, procedures, and regulations.

Responsibilities

Exhibit satisfactory knowledge of research techniques and procedures relating to the performance of clinical research, especially that 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.
Manage, prepare, and organize regulatory submissions and documents to necessary agencies.
Collaborate with Principal Investigator and the study team in the development, execution, administration and maintenance of protocols and clinical studies and 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.
Develop 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.
Coordinate with staff or students engaged in data collection to provide instruction on techniques, as well as consultation on project work.
Responsible for 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.
Perform library research on specified topics and prepare bibliographies and abstracts according to instructions.
Prepare materials for scientific reports to be written on research projects, including scientific abstracts, poster presentations, and peer-reviewed manuscripts.