To honor our promise to always put our patients first and to be ever mindful of each patients dignity and individuality, we must also be at the forefront of transformative discovery and innovation in psychiatric care.
Job Summary
The (CARL) Clinical Addictions Research Laboratory at the University of Chicago, (Director: Andrea C. King, Ph.D.), conducts human laboratory studies of responses to alcohol, cigarette smoking, and vaping, smartphone-based ecological momentary assessment of substance use in the natural environment, and behavioral and pharmacological interventions mainly focused on medically-compromised smokers. The full-time research assistant will provide support in all areas of investigation, including but not limited to: participant recruitment, interviewing and screening; conducting experimental sessions, tracking study progress/completion, database management, and follow-up assessments; providing administrative and infrastructure support in literature reviews, equipment calibration and maintenance, and organizing and filing records and study materials. Knowledge of MS Office (Word, Excel, etc.), communication skills, reliability, and detail-oriented work are necessary. Prior experience in human subjects testing, database and graphical packages, and statistics are desired.
Past research assistants have been accepted to strong PhD programs in clinical and experimental psychology, epidemiology, and medical school.
Responsibilities
Responsible for all aspects of research projects, including study recruitment and retention, participant screening and enrollment, data entry, and study-related communications among key personnel and participants.
Developing and disseminating study-specific advertisements, ensuring monthly recruiting and pacing goals are met.
Screening and scheduling study participants.
Conducting telephone and video-conferencing interviews with study applicants for eligibility determination and follow-up assessments.
Facilitates and monitors data collection, including obtaining subjective, objective (e.g. vital sign readings, etc.), biological (e.g. urine, blood, saliva, etc.), and performance (e.g. fine motor tasks, neurocognitive tasks, eye movement tasks, etc.) measures.
Provides administrative support (i.e. petty cash distribution, equipment inventory and maintenance, scientific literature reviews, etc.) and maintains detailed records of study and lab standard operating procedures.
Assists in development of data tables, graphs and charts and preparation of material for presentation.
Conduct screenings and participant interviews as needed, ensure database management, entry and verification of measures not obtained by computer, supervise and schedule sessions, perform clinical interviews as needed, and assist the lab manager on regulatory paperwork, scheduling and management of all disbursements and receipts.
Managing study supply inventory and ordering.
Creating subject mailings for materials related to their participation in the trial, including study medications and saliva drug screens.
Collects and enters data. Assists in analysis of data and with preparation of reports, manuscripts and other documents.
Complies with institution, state and federal regulatory policies, procedures, directives, and mandates.
Provides routine or standardized laboratory duties by collecting data in support of research projects under direct supervision.
Collects and enters data. Assists in analysis of data and with preparation of reports, manuscripts and other documents.
Performs other related work as needed.
Minimum Qualifications
Education:
Minimum requirements include vocational training, apprenticeships or the equivalent experience in related field (not typically required to have a four-year degree).
--- Work Experience:
Minimum requirements include knowledge and skills developed through --- Certifications:
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Preferred Qualifications
Experience:
Working in a complex academic medical center.
Preferred Competencies
Excellent professional and written communication skills.
Familiar with research studies.
Proficiency in MS Excel and electronic data capture (e.g., Redcap).
Experience in coding and statistical programs (i.e. R, Python, Java, SPSS, STATA, etc.).
Experience in interviewing and conducting experimental sessions in behavioral research.
Strong verbal and written communication skills.
Excellent attention to detail.
Working Conditions
Ability to work independently.
Application Documents
Resume (required)
Cover Letter (required)
When applying, the document(s) MUSTbe uploaded via the My Experience page, in the section titled Application Documents of the application.
Job Family
Research
Role Impact
Individual Contributor
FLSA Status
Non-Exempt
Pay Frequency
Biweekly
Scheduled Weekly Hours
40
Benefits Eligible
Yes
Drug Test Required
Yes
Health Screen Required
No
Motor Vehicle Record Inquiry Required
No
Posting Statement
The University of Chicago is an Affirmative Action/Equal Opportunity/Disabled/Veterans and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, national or ethnic origin, age, status as an individual with a disability, military or veteran status, genetic information, or other protected classes under the law. For additional information please see the University's Notice of Nondiscrimination.
Staff Job seekers in need of a reasonable accommodation to complete the application process should call 773-702-5800 or submit a request via Applicant Inquiry Form.
We seek a diverse pool of applicants who wish to join an academic community that places the highest value on rigorous inquiry and encourages a diversity of perspectives, experiences, groups of individuals, and ideas to inform and stimulate intellectual challenge, engagement, and exchange.
All offers of employment are contingent upon a background check that includes a review of conviction history. A conviction does not automatically preclude University employment. Rather, the University considers conviction information on a case-by-case basis and assesses the nature of the offense, the circumstances surrounding it, the proximity in time of the conviction, and its relevance to the position.
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