Talent.com

Study coordinator h1.location_city

[job_alerts.create_a_job]

Study coordinator • usa

[last_updated.last_updated_variable_hours]

Study Coordinator

University of ChicagoHyde Park Campus
[job_card.full_time]

SSD Institute for Mind and Biology: Staff and Temporary Employees.The Eating Disorders Program in the Department of Psychiatry and Behavioral Neuroscience at the University of Chicago (PI: Jennifer...[internal_linking.show_more]

 • [job_card.new]

Study Coordinator

The University of North Carolina at Chapel HillChapel Hill, NC, US
[job_card.permanent]

The UNC LCCC Cellular Therapy Program is seeking a study coordinator to facilitate complex investigational and FDA-approved cellular and gene therapies within according to federal regulations, Good...[internal_linking.show_more]

Senior Study Coordinator

MESO SCALE DIAGNOSTICS, LLCGaithersburg, MD, US
[job_card.full_time]

The Senior Study Coordinator (SC) provides support to the Bioanalytical Laboratory (BAL) staff for sample testing studies, including those performed under applicable elements of Good Laboratory Pra...[internal_linking.show_more]

Research Study Coordinator

Northwestern UniversityChicago, Illinois
[job_card.full_time]

Coordinates collection, analysis, processing & reporting of data & assists Principal Investigator (PI) in judging the validity of test data obtained in regard to biomedical &/or social-behavioral r...[internal_linking.show_more]

Research Study Coordinator / Phlebotomist

GI AssociatesWausau, WI, USA
[job_card.full_time]
[filters_job_card.quick_apply]

The Research Study Coordinator supports the successful implementation and coordination of clinical research studies by screening and enrolling participants, performing study-related procedures incl...[internal_linking.show_more]

Clinical Study Coordinator.

PSISouth Cook/Will County, Chicago, Illinois, US
[job_card.full_time]

The Site/Study Coordinator supports a medical institution in clinical trial-related activities.Protocol-specific tasks will be determined by the Principal Investigator, considering all local and fe...[internal_linking.show_more]

Clinical Study Coordinator

City of HopeDuarte, CA
[job_card.full_time]

Clinical Study Coordinator - Clinical Research (On-Site).Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes,...[internal_linking.show_more]

Sr. Study Coordinator

United BioSourceUS, Remote, US
[filters.remote]
[job_card.temporary]

As a pharmaceutical support industry leader,.At UBC we provide services to enhance the entire drug development process and commercialization lifecycle - From clinical trial support to real-world ev...[internal_linking.show_more]

Research Study Coordinator

Northwestern UniversityChicago, Illinois
[job_card.full_time]

Coordinates collection, analysis, processing & reporting of data & assists Principal Investigator (PI) in judging the validity of test data obtained in regard to biomedical &/or social-behavioral r...[internal_linking.show_more]

Research Study Coordinator

Boys TownPrimary Location: Omaha, Nebraska
[job_card.full_time]

Manages laboratory operations including regulatory and compliance documentation, recruitment of participants, and requisition of laboratory equipment and supplies.MAJOR RESPONSIBILITIES & DUTIES.En...[internal_linking.show_more]

Study Coordinator

SmithersGaithersburg, MD, US
[job_card.full_time]

Smithers PDS LLC (Pharmaceutical Development Services) brings new drugs to market by providing pre-clinical and clinical services for all phases of drug development.PDS works with customers to deve...[internal_linking.show_more]

Research Study Coordinator

Northwestern UniversityChicago, Illinois
[job_card.part_time]

Rinad Beidas’ team in the Department of Medical Social Sciences at Northwestern University Feinberg School of Medicine is seeking a Research Study Coordinator to assist our team with our diverse re...[internal_linking.show_more]

Research Study Coordinator

Henry Ford HealthDetroit, Michigan
[job_card.full_time]

Responsible for following established corporate policies and procedures to perform scientific investigative research and participate in carrying out research objectives; assist in the development o...[internal_linking.show_more]

Coordinator, Study Abroad

Mississippi State UniversityStarkville, MS, US
[job_card.full_time]

The position is responsible for coordinating all aspects of education abroad, including university risk management, promotion of study abroad programming, advising students of study abroad opportun...[internal_linking.show_more]

Study Coordinator

Howard UniversityWashington, DC, US
[job_card.full_time]

The Talent Acquisition department hires qualified candidates to fill positions which contribute to the overall strategic success of Howard University.Hiring staff “for fit” makes significant contri...[internal_linking.show_more]

Research Study Coordinator

University of ChicagoHyde Park Campus
[job_card.full_time]

SSD Psychology - Staff and Temporary Employees - Gallo.This is a research assistant position, the researcher will be hired by David Gallo, professor and PI, to work in his Memory Research Lab, in t...[internal_linking.show_more]

Clinical Study Coordinator

City of HopeNewnan, GA
[job_card.full_time]

City of Hope's mission is to make hope a reality for all touched by cancer and diabetes.Founded in 1913, City of Hope has grown into one of the largest and most advanced cancer research and treatme...[internal_linking.show_more]

Clinical Study Coordinator.

PSICleveland, Tennessee, US
[job_card.full_time]

The Site/Study Coordinator supports a medical institution in clinical trial-related activities.Protocol-specific tasks will be determined by the Principal Investigator, considering all local and fe...[internal_linking.show_more]

Research Study Coordinator

University of Maryland Eastern ShorePrincess Anne, MD, US
[job_card.full_time]

The Research Study Coordinator will play a pivotal role in the AI-FOR-U project, supporting the Principal Investigator by ensuring that communications, required reports, and project activities are ...[internal_linking.show_more]

Study Coordinator

Study Coordinator

University of ChicagoHyde Park Campus
[job_card.variable_hours_ago]
[job_preview.job_type]
  • [job_card.full_time]
[job_card.job_description]

Department

SSD Institute for Mind and Biology: Staff and Temporary Employees


About the Department

The Eating Disorders Program in the Department of Psychiatry and Behavioral Neuroscience at the University of Chicago (PI: Jennifer Wildes) and the Bakkour Memory and Decision Laboratory in the Department of Psychology (PI: Akram Bakkour) offer the ideal setting to conduct impactful cognitive neuroscience research with clinical implications. The two units offer ample opportunity for specialized training and exposure to a diversity of methods and approaches to research.


Job Summary

The job performs routine assignments related to scientific research projects. Ensures compliance of research activities with institutional, state, and federal regulatory policies, procedures, directives and mandates. Analyzes possible solutions using standard procedures. Writes articles, reports and manuscripts. Assists in drafting presentations on research findings.

The Eating Disorders Program in the Department of Psychiatry and Behavioral Neuroscience at the University of Chicago (PI: Jennifer Wildes) and the Bakkour Memory and Decision Laboratory in the Department of Psychology (PI: Akram Bakkour) are seeking a full-time Study Coordinator for a NIMH-funded project. The project aims to uncover cognitive and neural mechanisms underlying maladaptive food-choice behavior in anorexia nervosa using behavioral tasks, eye tracking, fMRI, and computational modeling approaches.
The Study Coordinator will provide technical and administrative support for research activities and will be responsible for the day-to-day management and coordination of the project.

Responsibilities

  • Coordinate and manage daily research operations and data collection activities.
  • Assist in preparing IRB protocols, amendments, and regulatory documentation.
  • Monitor compliance with institutional, state, and federal regulatory policies and procedures.
  • Coordinate participant recruitment (clinical and healthy populations) and scheduling.
  • Maintain and organize study records (e.g., consent forms, screening data, study logs).
  • Conduct participant interviews and administer behavioral and cognitive tasks.
  • Set up and assist with eye-tracking and fMRI data collection sessions.
  • Coordinate medical exams and laboratory assessments as needed.
  • Manage and maintain data collection files and databases.
  • Assist with data processing, analysis, and quality control.
  • Provide general administrative support and coordinate with laboratory staff, trainees, and investigators.
  • Maintains technical and administrative support for a research project.
  • Analyzes and maintains data and/or specimens. Conducts literature reviews. Assists with preparation of reports, manuscripts and other documents.
  • Perform other related duties as needed.


Minimum Qualifications

Education:

Minimum requirements include a college or university degree in related field.


Work Experience:

Minimum requirements include knowledge and skills developed through < 2 years of work experience in a related job discipline.


Certifications:

---

Preferred Qualifications

Education:

  • Bachelor’s degree in psychology, neuroscience, cognitive science, or a related field.

Experience:

  • Relevant research experience.
  • Experience supporting research projects in a laboratory or clinical research environment.
  • Working knowledge of research methods and basic statistical analyses.
  • Prior experience in psychopathology and/or cognitive neuroscience research.
  • Experience with human subjects research protocols (IRB, consent procedures, HIPAA).
  • Experience managing or coordinating research studies.

Preferred Competencies

  • Communicates effectively and professionally with participants, staff, and investigators.
  • Highly organized and detail-oriented; able to exercise good judgment and take initiative.
  • Able to work independently as well as collaboratively in a team environment.
  • Strong time management and ability to manage multiple tasks and priorities.
  • Demonstrates accountability and reliability in managing responsibilities.
  • Fosters collaboration and positive working relationships.

Working Conditions

  • Laboratory and clinical research environment.
  • Interaction with clinical populations (including individuals with eating disorders).
  • May involve exposure to MRI scanning environments and standard laboratory procedures.
  • Ability to sit or stand for extended periods and use computers for data collection and analysis.
  • Full-time position based at the University of Chicago.
  • Initial appointment is for one year, with the possibility of renewal.
  • Preferred start date between June and August 2026.
  • Candidates must be eligible to work in the United States.

Application Documents

  • Resume/CV (required)
  • Cover letter (required)
  • References (required)


When applying, the document(s) MUST be uploaded via the My Experience page, in the section titled Application Documents of the application.


Job Family

Research


Role Impact

Individual Contributor


Scheduled Weekly Hours

37.5


Drug Test Required

No


Health Screen Required

No


Motor Vehicle Record Inquiry Required

No


Pay Rate Type

Hourly


FLSA Status

Non-Exempt


Pay Range

$25.71 - $33.28

The included pay rate or range represents the University’s good faith estimate of the possible compensation offer for this role at the time of posting.


Benefits Eligible

Yes

The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off. Information about the benefit offerings can be found in theBenefits Guidebook.


Posting Statement

The University of Chicago is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, or expression, national or ethnic origin, shared ancestry, 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.

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.

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.

The University of Chicago's Annual Security & Fire Safety Report (Report) provides information about University offices and programs that provide safety support, crime and fire statistics, emergency response and communications plans, and other policies and information. The Report can be accessed online at: . Paper copies of the Report are available, upon request, from the University of Chicago Police Department, 850 E. 61st Street, Chicago, IL 60637.