Director, Clinical Research Systems and Compliance jobs in United States
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University of Chicago · 7 hours ago

Director, Clinical Research Systems and Compliance

The University of Chicago is seeking a Director for the Office of Clinical Research, responsible for managing clinical research systems and compliance. The role involves overseeing multiple teams, ensuring efficient operations, and driving strategic initiatives to enhance clinical research processes and compliance standards.

Higher Education
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H1B Sponsor Likelynote

Responsibilities

Act as business system owner for CTMS, OnCore, and the central intake system, ServiceNow. Responsibilities include but are not limited to driving continuous improvement through development of a multi-year roadmap and partnering with IT teams responsible for technical management
Provide strategic oversight and responsibility for the coverage-analysis service line, ensuring high-quality day-to-day operations, compliance with CMS requirements, ongoing process improvements, and sustainable growth of the unit
Oversee the central study intake platform and the staff responsible for intake operations, ensuring efficient study triage, accurate data capture, and alignment with enterprise research workflows
Manage the technology and education pillar for research systems, including the design of workflows, development of training materials, and delivery of ongoing education programs for OCR offices and end users. Develop and oversee a formalized CTMS training program for new and existing staff within the unit and affiliated partners
Lead, mentor, and develop a high-performing team of clinical research professionals, fostering a collaborative and innovative team culture
Provide operational guidance to internal teams and other institutional stakeholders to ensure alignment of operations and strategy
Develop and maintain Standard Operating Procedures and ensure adherence across the clinical research enterprise. Collaborate with institutional stakeholders to ensure compliance and optimization of processes
Employ data metrics to deliver insights and recommendations that inform strategic initiatives throughout the systems application lifecycle
Identify and implement best practices for clinical research workflows. Utilize process-improvement methodologies to enhance efficiency and effectiveness in study execution
Partner with finance, compliance, research administration, and other stakeholders to ensure seamless integration of clinical research activities as it relates to enterprise system optimization
Provide expert guidance on clinical research operations processes and serve as a resource for team members and collaborators across the institution
Monitor trends, changes, and new developments in federal, state, and local research regulations, laws, and guidance documents to ensure research operations and processes adhere to current requirements and industry best practices
Manages managers and professional staff to monitor financial transactions, revenues and expenditures for clinical research trials. Ensures all data is accurately recorded, utilizing institutional (accounting and research) policies
Monitors project management and ensures that clinical trials are conducted in compliance with federal and institutional regulations. Manages, monitors and reports project budgets and annual projections
Develops departmental plans, including strategic initiatives for the department, in collaboration with departmental and divisional leadership
Advises faculty and research staff on all facets of clinical trial research management, including research conduct and compliance
Performs other related work as needed

Qualification

Clinical Trial Management SystemMedicare Coverage AnalysisICH E6 Good Clinical PracticesProcess ImprovementData Metrics AnalysisTeam ManagementMicrosoft Office SuiteOrganizational SkillsCommunication SkillsAttention to Detail

Required

Minimum requirements include a college or university degree in related field
Minimum requirements include knowledge and skills developed through 7+ years of work experience in a related job discipline
Act as business system owner for CTMS, OnCore, and the central intake system, ServiceNow
Provide strategic oversight and responsibility for the coverage-analysis service line, ensuring high-quality day-to-day operations, compliance with CMS requirements, ongoing process improvements, and sustainable growth of the unit
Oversee the central study intake platform and the staff responsible for intake operations, ensuring efficient study triage, accurate data capture, and alignment with enterprise research workflows
Manage the technology and education pillar for research systems, including the design of workflows, development of training materials, and delivery of ongoing education programs for OCR offices and end users
Lead, mentor, and develop a high-performing team of clinical research professionals, fostering a collaborative and innovative team culture
Provide operational guidance to internal teams and other institutional stakeholders to ensure alignment of operations and strategy
Develop and maintain Standard Operating Procedures and ensure adherence across the clinical research enterprise
Employ data metrics to deliver insights and recommendations that inform strategic initiatives throughout the systems application lifecycle
Identify and implement best practices for clinical research workflows
Partner with finance, compliance, research administration, and other stakeholders to ensure seamless integration of clinical research activities as it relates to enterprise system optimization
Provide expert guidance on clinical research operations processes and serve as a resource for team members and collaborators across the institution
Monitor trends, changes, and new developments in federal, state, and local research regulations, laws, and guidance documents to ensure research operations and processes adhere to current requirements and industry best practices
Manages managers and professional staff to monitor financial transactions, revenues and expenditures for clinical research trials
Monitors project management and ensures that clinical trials are conducted in compliance with federal and institutional regulations
Develops departmental plans, including strategic initiatives for the department, in collaboration with departmental and divisional leadership
Advises faculty and research staff on all facets of clinical trial research management, including research conduct and compliance

Preferred

Advanced degree in the sciences
Experience with Clinical Trial Management System (CTMS) and other enterprise solutions for research administration
Experience managing a team of individuals
Medicare Coverage Analysis knowledge and experience
Knowledge of policies, procedures and legislation concerning human subjects in research and the Code of Federal Regulations
Expert knowledge of ICH E6 Good Clinical Practices and regulations of clinical research set forth in the Code of Federal Regulations, the Office for Human Research Protections, Food and Drug Administration, National Institutes of Health and Center for Medicare and Medicaid Services or other relevant agencies
Ability to interpret research protocol information in relation to federal requirements and internal policies, exercise sound judgment and make recommendations and/or decisions regarding research policies
Expert knowledge of CMS billing rules (NCD, LCD) and Medicare Coverage Analysis best practices
Experience leading highly functioning teams and overseeing managers and independent contributors
Proven record of building effective working relationships across functions as well as support effective partnerships with key groups and individuals
Expert knowledge of Microsoft Word, Excel, Outlook and PowerPoint software
Excellent organizational skills
Ability to work independently and drive work forward
Attention to detail
Ability to prepare accurate documentation and maintain confidential material and information
Excellent written and verbal communication skills to effectively interface with pharmaceutical industry, the hospital and departments within the Division
Ability to resolve issues, problem solve and make effective recommendations

Benefits

Health, retirement, and paid time off

Company

University of Chicago

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One of the world’s great intellectual destinations, the University of Chicago empowers scholars and students to ask tough questions, cross disciplinary boundaries, and challenge conventional thinking to enrich human life around the globe.

H1B Sponsorship

University of Chicago has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (341)
2024 (318)
2023 (285)
2022 (233)
2021 (179)
2020 (172)

Funding

Current Stage
Late Stage

Leadership Team

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Benedicte Nolens
Distinguished Executive in Residence
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