The University Of Chicago
Clinical Research Coordinator I
The University Of Chicago, Chicago, Illinois, United States, 60290
Department
BSD OBG - Generalists - PCORI Research About the Department
The Department of Obstetrics and Gynecology has 140 clinical providers, providing care at the main hospital in Hyde Park and seven off-site locations. We have more than 68,000 outpatient visits, 28,000 ultrasound visits, 2,800 deliveries, and 3,300 surgeries per year. Teaching, research, and high-quality clinical care are top priorities. The residency and fellowship programs are highly ranked, with a history of training healthcare leaders. The department has a significant research enterprise, including population health studies and laboratory research in tumor biology, fibroid research, and hypertensive diseases in pregnancy. The Section of Family Planning has established CI3, a research center focused on reproductive policy and sexual and reproductive health innovations. The department was ranked #16 in the 2022-2023 U.S. News & World Report. This at-will position is funded by contractual grant funding, which is renewed based on the grantor’s provisions. Employment depends on continued funding and satisfactory job performance. Job Summary
The Clinical Research Coordinator performs routine tasks related to documenting and reporting basic clinical studies. Supports decisions impacting clinical research across the university. This role supports a PCORI-funded project examining the benefits of breastfeeding peer counseling to reduce disparities among Black and Latine women. Under supervision, the Research Associate works with principal investigators, research staff, and the project manager to support patient recruitment and assessment for a multisite randomized trial. Responsibilities include obtaining consent, administering exams and questionnaires, data entry, chart abstraction, and assisting in presentation and publication preparation. The coordinator is accountable for implementing and evaluating patient care within research protocols, maintaining collaborative relationships, and working on-site at the university campus. Responsibilities
Participate in staff and departmental meetings. Engage in ongoing professional development through workshops and seminars. Provide patient care based on individual needs and criteria. Ensure compliance with research guidelines, including IRB protocols, consent regulations, and safety reporting. Maintain documentation with IRB and funding agencies. Assist in developing study forms, databases, and data collection strategies. Understand and adhere to study protocols. Support research initiation and coordination with other departments. Recruit, enroll, and consent patients for studies. Administer questionnaires and maintain communication with participants. Abstract charts and ensure accurate study treatment and drug accountability. Monitor clinical parameters, document adverse events, and report deviations. Ensure confidentiality and maintain organized documentation. Manage databases and assist in data analysis and manuscript preparation. Provide technical and administrative support for research projects. Support quality assurance and data collection efforts. Perform other related tasks as needed. Minimum Qualifications
Education: College or university degree in a related field. Work Experience: Less than 2 years in a related discipline. Certifications: Not specified. Preferred Qualifications
Bachelor’s degree in Social Science or related field. Research and data management experience. Research certification after 2 years preferred. Preferred Competencies
Knowledge of customer service standards and policies. Understanding of relevant laws and regulations. Exceptional customer service, teamwork, professionalism, organization, and communication skills. Bilingual Spanish-English preferred. Working Conditions
Office/clinic setting. Ability to sit, stand, and lift up to 15 lbs. Application Documents
Resume (required) Cover Letter (preferred) Applications must be uploaded via the My Experience page under 'Application Documents.' Additional Details
Job family: Research Impact: Individual Contributor Hours: 40/week Drug Test: Yes Health Screen: Yes Motor Vehicle Record Inquiry: No Pay Range: $50,000 - $65,000 Benefits: Eligible, including health, retirement, and paid time off. Equal Opportunity Statement
The University of Chicago is an equal opportunity employer. Reasonable accommodations are available for applicants with disabilities. Employment is contingent on background checks. For safety information, visit the university’s security report online.
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BSD OBG - Generalists - PCORI Research About the Department
The Department of Obstetrics and Gynecology has 140 clinical providers, providing care at the main hospital in Hyde Park and seven off-site locations. We have more than 68,000 outpatient visits, 28,000 ultrasound visits, 2,800 deliveries, and 3,300 surgeries per year. Teaching, research, and high-quality clinical care are top priorities. The residency and fellowship programs are highly ranked, with a history of training healthcare leaders. The department has a significant research enterprise, including population health studies and laboratory research in tumor biology, fibroid research, and hypertensive diseases in pregnancy. The Section of Family Planning has established CI3, a research center focused on reproductive policy and sexual and reproductive health innovations. The department was ranked #16 in the 2022-2023 U.S. News & World Report. This at-will position is funded by contractual grant funding, which is renewed based on the grantor’s provisions. Employment depends on continued funding and satisfactory job performance. Job Summary
The Clinical Research Coordinator performs routine tasks related to documenting and reporting basic clinical studies. Supports decisions impacting clinical research across the university. This role supports a PCORI-funded project examining the benefits of breastfeeding peer counseling to reduce disparities among Black and Latine women. Under supervision, the Research Associate works with principal investigators, research staff, and the project manager to support patient recruitment and assessment for a multisite randomized trial. Responsibilities include obtaining consent, administering exams and questionnaires, data entry, chart abstraction, and assisting in presentation and publication preparation. The coordinator is accountable for implementing and evaluating patient care within research protocols, maintaining collaborative relationships, and working on-site at the university campus. Responsibilities
Participate in staff and departmental meetings. Engage in ongoing professional development through workshops and seminars. Provide patient care based on individual needs and criteria. Ensure compliance with research guidelines, including IRB protocols, consent regulations, and safety reporting. Maintain documentation with IRB and funding agencies. Assist in developing study forms, databases, and data collection strategies. Understand and adhere to study protocols. Support research initiation and coordination with other departments. Recruit, enroll, and consent patients for studies. Administer questionnaires and maintain communication with participants. Abstract charts and ensure accurate study treatment and drug accountability. Monitor clinical parameters, document adverse events, and report deviations. Ensure confidentiality and maintain organized documentation. Manage databases and assist in data analysis and manuscript preparation. Provide technical and administrative support for research projects. Support quality assurance and data collection efforts. Perform other related tasks as needed. Minimum Qualifications
Education: College or university degree in a related field. Work Experience: Less than 2 years in a related discipline. Certifications: Not specified. Preferred Qualifications
Bachelor’s degree in Social Science or related field. Research and data management experience. Research certification after 2 years preferred. Preferred Competencies
Knowledge of customer service standards and policies. Understanding of relevant laws and regulations. Exceptional customer service, teamwork, professionalism, organization, and communication skills. Bilingual Spanish-English preferred. Working Conditions
Office/clinic setting. Ability to sit, stand, and lift up to 15 lbs. Application Documents
Resume (required) Cover Letter (preferred) Applications must be uploaded via the My Experience page under 'Application Documents.' Additional Details
Job family: Research Impact: Individual Contributor Hours: 40/week Drug Test: Yes Health Screen: Yes Motor Vehicle Record Inquiry: No Pay Range: $50,000 - $65,000 Benefits: Eligible, including health, retirement, and paid time off. Equal Opportunity Statement
The University of Chicago is an equal opportunity employer. Reasonable accommodations are available for applicants with disabilities. Employment is contingent on background checks. For safety information, visit the university’s security report online.
#J-18808-Ljbffr