Description:
We are searching for a reliable, motivated, detail-oriented, collaborative team member to assist with clinical studies of mood disorders. The study coordinator will work closely with the principal investigator, other research staff, clinical staff, university administrators, and regulatory entities to ensure that all research activities are performed efficiently, ethically, and in accordance with federal and university regulations, policies, and guidelines. The ideal candidate will have excellent interpersonal, verbal, and writing skills; some experience with human-subjects research; and a strong interest in creating new knowledge that will ultimately improve treatment and prevention of mental illness.
University of Utah Job ID# PRN15202B, Psychiatry - Research
WORK SCHEDULE: Full time, 40 hours/week.
COMPENSATION: $31,600 to $38,299 DOE. Strong benefit package including tuition reduction program, Bus/TRAX pass, retirement and health plan options.
RESPONSIBILITIES:
• Attend investigator and team meetings to manage the day-to-day activities of studies
• Assist the principal investigator in developing protocols, data collection tools, and other study materials
• Prepare applications, amendments, reports, and continuing review documents for the IRB, FDA, and other regulatory agencies
• Establish and organize study files, including regulatory binders, participant folders, and study databases
• Maintain up-to-date training, education, and certification as required by protocols
• Assist the principal investigator in the training, education, and certification of students, post-docs, and other research trainees
• Schedule research meetings for the principal investigator and co-investigators
• Work with research staff and clinical staff to screen and recruit potential participants
• Schedule and register participants for study visits, including evaluations, interventions, and neuroimaging
• Assist the principal investigator in collection of clinical data, biospecimens, and neuroimaging data
• Develop and maintain rapport with participants during longitudinal studies
• Ensure that appropriate funding sources are billed for research activities
• Order supplies and equipment for study activities
May maintain contact with IRB and prepare and submit IRB documents. May ensure proper collection, processing and shipment of specimens. May perform functions required of the Clinical Research Assistant as necessary.
Qualifications:
Bachelor’s degree in a related field, or equivalency required. IRB CITI Course in the Protection of Human Research subjects certificate obtained within six months of hire and demonstrated human relations and effective communication skills are also required. Some departments may require IATA DGR training within six months.
PREFERENCES:
• Excellent interpersonal, verbal, and writing skills
• Experience with human-subjects research
• Strong interest in creating new knowledge that will ultimately improve treatment and prevention of mental illness
Application Instructions:
PLEASE APPLY ONLINE THROUGH THE UNIVERSITY OF UTAH SYSTEM TO BE CONSIDERED FOR THIS JOB:
http://utah.peopleadmin.com/postings/68781
EQUAL EMPLOYMENT OPPORTUNITY
The University of Utah is an Affirmative Action/Equal Opportunity employer. Upon request, reasonable accommodations in the application process will be provided to individuals with disabilities. Please contact the Office of Equal Opportunity and Affirmative Action, 201 S. Presidents Cr., Rm 135, (801) 581-8365 (V/TDD), for further information or to request an accommodation. The University of Utah is committed to diversity in its workforce. Women and minorities are encouraged to apply.