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BSD IPP - Connect

About the Department

The newly created Institute for Population and Precision Health (IPPH), located in the Biological Sciences Division, will integrate 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

This position provides technical support activities related to 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

• Performs blood draws both in the clinic and in community, including in-home, settings.
• Collects and maintains biometric data and biospecimens.
• Introduces patients at the UCMC, and in the communities in the Community Mobile Clinic Van, to the research study. Answers questions pertaining to participation and consent, and may assist in administering tests and/or questionnaires following protocols.
• Performs blood draws and processes blood and urine samples.
• Responsible for packaging and shipping biological samples to an outside lab.
• Completes all activities by strictly following Good Clinical Practices (GCP) and all relevant, current local, state, and federal laws, regulations, guidance, policy and procedure, developed by the UChicago Institutional Review Board (IRB), Food and Drug Administration (FDA) Code of Federal Regulations (CFR), and the International Conference on Harmonization (ICH).
• Maintains detailed records of results which may include collecting, extracting and entering data; and/or preparing basic charts and graphs.
• Responsible for other duties such as preparing charts for the participant visits, setting up and cleaning the exam rooms before and after the visits, entering data as needed, performing data and equipment quality control checks, etc.
• Performs specific protocol procedures (specimens and data management, survey/questionnaire administration and the like) required to conduct the study and retain research subjects.
• Understands protocols and may collect information about adverse events (AEs), identified in the protocol or investigator brochure.
• Prepares for or participate in quality assurance audits under supervision or following specific protocol procedures.
• Participates in study-related documentation, such as protocol worksheets, procedural manuals, adverse event repo ts, institutional review board documents, or progress reports.
• 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).

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Work Experience:

Minimum requirements include knowledge and skills developed through ---

Certifications:

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Preferred Qualifications

Education:

• Bachelor\'s degree in epidemiology, public health or closely related field.

Experience:

• One yearof relevant research experience including experience with outreach efforts, study recruitment, and collecting biometric data.

Licenses and Certifications:

• Phlebotomy certificate.

Technical Skills or Knowledge:

• Microsoft Office.
• Knowledge in relevant scientific field.
• Research techniques or methods.
• Regulatory policies and procedures.

Preferred Competencies

Analytical skills.

Problem-solving skills.

Attention to detail.\<