Clinical Research Coordinator 2, Nutrition for Precision Health

Department
BSD IPP-NPH

About the Department
The Institute for Population and Precision Health (IPPH), located in the Biological Sciences Division, integrates a wide spectrum of factors such as human health behaviors, environmental factors, social and economic factors, policies and genetic determinants of health, into studies focused on the treatment and prevention of disease, as well as the maintenance of wellness. Leveraging and integrating the University of Chicago's considerable institutional strength in population science with research spanning diverse fields such as genetic medicine, cancer epidemiology, microbiome, and epigenomics, the Institute will have the common goal of improving human health outcomes. Another major goal of the Institute will be to develop a new multidisciplinary training program to equip researchers with emerging tools and methods to conduct precision health research within a population health framework. Our faculty lead research projects in biostatistics, epidemiology and health services research and participate in interdisciplinary teams with faculty in other departments to address complex problems in health and healthcare, in our communities and around the globe.

Job Summary
UChicago is part of a mega-National Institutes of Health (NIH) program that aims to be the first comprehensive study to investigate precision nutrition. The goal is to develop algorithms to predict individual responses to food and dietary routines. Precision nutrition, also known as personalized nutrition, will move away from 'one-size-fits-all' diet recommendations and create a customized diet plan for people based on individual differences, such as genetics and metabolism.

The Clinical Research Coordinator 2 compiles, documents, analyzes, and reports on clinical research data. Provides input to support the strategic, administrative, operational, and financial decisions that impact clinical research conducted across the University.

This at-will position is wholly or partially funded by contractual grant funding which is renewed under provisions set by the grantor of the contract. Employment will be contingent upon the continued receipt of these grant funds and satisfactory job performance.

Responsibilities

• Coordination and management quality control for observational and interventional, including both clinic and community-based studies, within the Institute for Population and Precision Health.
• This may include multi-institutional and some international studies, many of which are federally funded or funded by pharmaceutical sponsors.
• This may include oversight of the collection of clinical data, survey data, environmental data, and associated samples and biospecimens.
• Coordination; Institutional Review Board (IRB) preparation; development of data collection instruments; assurance of implementation accuracy and study staff compliance; and continuous reporting on milestones, success, and challenges to study leadership.
• Assist with subject engagement, screening, recruitment, consent, data and specimen collection, and subject follow-up and retention activities.
• Monitor study participants, schedule, and conduct study-related procedures (eg. interviews, phlebotomies, and follow-ups) and establish data quality control checks).
• Work with the Scientific Directors and Research Manager in the planning, development, and evaluation of research.
• Coordination of data acquisition, entry, QC, and query response.
• Assist in the development of new projects and preparation of study reports, and manuscripts for publication.
• Assist in the preparation of presentations, media, and curricular materials relating to research.
• Accountable for all tasks in moderately complex clinical studies.
• Assists with various professional, organizational, and operational tasks under moderate supervision.
• Facilitates and participates in the daily activities of moderately complex clinical studies and performs various activities including patient data retrieval, documenting clinical research records, and participation in program audits.
• Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples with a limited to moderate degree of independence. Contributes to the problem solving on assigned clinical research studies and tasks.
• Performs other related work 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 2-5 years of work experience in a related job discipline.

Certifications:

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Preferred Qualifications

Education:

• Master's degree in public health, epidemiology or related field.

Preferred Competencies

• Working knowledge of nutrition science and its application to clinical research, including relevant scientific principles, methodologies, and current research practices.
• Knowledge of clinical research techniques, methodologies, and procedures, with the ability to apply appropriate methods to support high-quality research outcomes.
• Strong data management skills and attention to detail; familiarity Good Clinical Practices (GCP); extensive knowledge of Microsoft Word, Excel, and Adobe Acrobat; understanding of federal research regulations and human research protections; ability to participate in protocol review and evaluate clinical trials.
• Strong analytical and problem-solving skills , with the ability to assess complex research issues, identify solutions, and exercise sound judgement.
• Ability to prioritize multiple tasks, manage time efficiently, meet deadlines, and maintain strong organizational skills; work independently; learn and develop new skills.
• Ability to communicate in writing and orally; follow written and verbal instructions; comprehend and read complex technical and clinical documents.
• Ability to develop and manage interpersonal relationships; work effectively, independently, or as part of a team; collaborate with faculty and divisional clinical research infrastructure; demonstrate excellent interpersonal skills.
• Ability to work independently and as part of a team.
• Knowledge of Microsoft Office.
• Ability to train, mentor, and develop frontline research staff while promoting adherence to research protocols, quality standards, and operational objectives.

Working Conditions

• Office, clinic, and community setting.

Application Documents

• Resume (required)
• Cover Letter (preferred)

The University of Chicago uses AI-assisted tools to streamline and augment some recruitment processes; however, AI is not used to make hiring decisions.

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
40

Drug Test Required
Yes

Health Screen Required
Yes

Motor Vehicle Record Inquiry Required
No

Pay Rate Type
Salary

FLSA Status
Exempt

Pay Range
$60,000.00 - $75,000.00
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 the Benefits 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.

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