Human Subject Protection (IRB); Training and Education; Regulatory and Contract Oversight; Quality ... and contractual agreements. * Maintain an understanding of Medicare's Clinical Trial Policy (NCD ...
Human Subject Protection (IRB); Training and Education; Regulatory and Contract Oversight; Quality ... and contractual agreements. * Maintain an understanding of Medicare's Clinical Trial Policy (NCD ...
Clinical Research Financial Analyst
Chicago, IL · On-site +1
Human Subject Protection (IRB); Training and Education; Regulatory and Contract Oversight; Quality ... and contractual agreements. * Maintain an understanding of Medicare's Clinical Trial Policy (NCD ...
Clinical Research Financial Analyst
Chicago, IL · On-site +1
Human Subject Protection (IRB); Training and Education; Regulatory and Contract Oversight; Quality ... and contractual agreements. * Maintain an understanding of Medicare's Clinical Trial Policy (NCD ...
Substance Use Disorder Prevention Analyst
Annapolis, MD · On-site
$30/hr
Behavioral Health | System Training, Education and Prevention Services Full-Time County Contractual ... IRB) process. Develop educational materials for the general public to provide opioid misuse ...
Substance Use Disorder Prevention Analyst
Annapolis, MD · On-site
$30/hr
Behavioral Health | System Training, Education and Prevention Services Full-Time County Contractual ... IRB) process. Develop educational materials for the general public to provide opioid misuse ...
Clinical Contracts Analyst (REMOTE)
Minneapolis, MN · On-site +1
$72K - $87K/yr
... IRB oversight, and other reimbursable costs for clinical trials. • Manage contractual and ... analytics, reporting, and business intelligence support for clinical trials. • Track timelines ...
Clinical Contracts Analyst (REMOTE)
Minneapolis, MN · On-site +1
$72K - $87K/yr
... IRB oversight, and other reimbursable costs for clinical trials. • Manage contractual and ... analytics, reporting, and business intelligence support for clinical trials. • Track timelines ...
Clinical Contracts Analyst (REMOTE)
Minneapolis, MN · Remote
$72K - $87K/yr
... fees, IRB oversight, and other reimbursable costs for clinical trials. Manage contractual and ... Provide data management, analytics, reporting, and business intelligence support for clinical ...
Clinical Contracts Analyst (REMOTE)
Minneapolis, MN · Remote
$72K - $87K/yr
... fees, IRB oversight, and other reimbursable costs for clinical trials. Manage contractual and ... Provide data management, analytics, reporting, and business intelligence support for clinical ...
Ability to understand contractual issues, relevant contract law and health care policy within ... Board (IRB), and Institutional Animal Care and Use Committee approvals (IACUC). * Ensures ...
Ability to understand contractual issues, relevant contract law and health care policy within ... Board (IRB), and Institutional Animal Care and Use Committee approvals (IACUC). * Ensures ...
Research Contract Analyst
Houston, TX · On-site
Ability to understand contractual issues, relevant contract law and health care policy within ... Board (IRB), and Institutional Animal Care and Use Committee approvals (IACUC). * Ensures ...
Research Contract Analyst
Houston, TX · On-site
Ability to understand contractual issues, relevant contract law and health care policy within ... Board (IRB), and Institutional Animal Care and Use Committee approvals (IACUC). * Ensures ...
... analyses, coverage analyses, and research billing grids. * Collaborates with investigators ... IRB, finance offices, and institutional service providers to ensure alignment across contractual ...
... analyses, coverage analyses, and research billing grids. * Collaborates with investigators ... IRB, finance offices, and institutional service providers to ensure alignment across contractual ...
... analyses, coverage analyses, and research billing grids. * Collaborates with investigators ... IRB, finance offices, and institutional service providers to ensure alignment across contractual ...
... analyses, coverage analyses, and research billing grids. * Collaborates with investigators ... IRB, finance offices, and institutional service providers to ensure alignment across contractual ...
... contractual timelines and expectations. * Partner with fiscal staff to manage reimbursement ... data analysis, regulatory compliance, and IRB processes. * Demonstrated ability to work ...
... contractual timelines and expectations. * Partner with fiscal staff to manage reimbursement ... data analysis, regulatory compliance, and IRB processes. * Demonstrated ability to work ...
Research Coordinator 3 (Temporary)
Seattle, WA · On-site +1
$87K/yr
... contractual timelines and expectations. * Partner with fiscal staff to manage reimbursement ... data analysis, regulatory compliance, and IRB processes. * Demonstrated ability to work ...
Research Coordinator 3 (Temporary)
Seattle, WA · On-site +1
$87K/yr
... contractual timelines and expectations. * Partner with fiscal staff to manage reimbursement ... data analysis, regulatory compliance, and IRB processes. * Demonstrated ability to work ...
SR Clinical Research Coordinator
$28.50 - $38/hr
... Review Board (IRB), human resources, contracts and grants) and elsewhere (industry sponsors ... Exceptional analytical skills to evaluate the importance and urgency of problems; excellent ...
SR Clinical Research Coordinator
$28.50 - $38/hr
... Review Board (IRB), human resources, contracts and grants) and elsewhere (industry sponsors ... Exceptional analytical skills to evaluate the importance and urgency of problems; excellent ...
Project Manager
Syracuse, NY · On-site
$66K - $70K/yr
... contractual requisites; and external market analyses. Staff Level S5 FLSA Status Exempt Hours ... IRB review, study design, analysis, and research-related software programs (reference management ...
Project Manager
Syracuse, NY · On-site
$66K - $70K/yr
... contractual requisites; and external market analyses. Staff Level S5 FLSA Status Exempt Hours ... IRB review, study design, analysis, and research-related software programs (reference management ...
Associate Grants Officer
Evanston, IL · On-site
$8/hr
... analysis of contractual issues including the review, redlining, and negotiation of government ... Solicit input from principal investigators and other central administrative offices, such as IRB ...
Associate Grants Officer
Evanston, IL · On-site
$8/hr
... analysis of contractual issues including the review, redlining, and negotiation of government ... Solicit input from principal investigators and other central administrative offices, such as IRB ...
Clinical Research Data Coordinator - Neuroscience- Atlantic Health - Overlook Medical Center
Summit, NJ · On-site
$25.75 - $34.25/hr
... and contractual requirements. Creates databases and data collection tools as needed for ... Board (IRB) within the required time frame dictated by the IRB of record. Prepares reports ...
Clinical Research Data Coordinator - Neuroscience- Atlantic Health - Overlook Medical Center
Summit, NJ · On-site
$25.75 - $34.25/hr
... and contractual requirements. Creates databases and data collection tools as needed for ... Board (IRB) within the required time frame dictated by the IRB of record. Prepares reports ...
This at-will position is wholly or partially funded by contractual grant funding, which is renewed ... IRB requirements and institutional compliance standards. * Advanced analytical and critical ...
This at-will position is wholly or partially funded by contractual grant funding, which is renewed ... IRB requirements and institutional compliance standards. * Advanced analytical and critical ...
Sr Clinical Research Coordinator Clinical Research Network Office
Berkeley, CA · On-site
$29.75 - $39.50/hr
The incumbent may have central responsibility for assisting with IRB approval and compliance ... Design and perform ad-hoc performance analysis of the projects and the project staff * Build ...
Sr Clinical Research Coordinator Clinical Research Network Office
Berkeley, CA · On-site
$29.75 - $39.50/hr
The incumbent may have central responsibility for assisting with IRB approval and compliance ... Design and perform ad-hoc performance analysis of the projects and the project staff * Build ...
The incumbent may have central responsibility for assisting with IRB approval and compliance ... Exceptional analytical skills to evaluate the importance and urgency of problems; excellent ...
The incumbent may have central responsibility for assisting with IRB approval and compliance ... Exceptional analytical skills to evaluate the importance and urgency of problems; excellent ...
SR Clinical Research Coordinator
San Francisco, CA · On-site
$28.50 - $38/hr
... Review Board (IRB), human resources, contracts and grants) and elsewhere (industry sponsors ... Design and perform ad-hoc performance analysis of the projects and the project staff * Build ...
SR Clinical Research Coordinator
San Francisco, CA · On-site
$28.50 - $38/hr
... Review Board (IRB), human resources, contracts and grants) and elsewhere (industry sponsors ... Design and perform ad-hoc performance analysis of the projects and the project staff * Build ...
Performs preliminary study analysis under the direction of the Principal Investigator or senior ... IRB. * Ensures consent process is performed and documented in compliance with regulations and ...
Performs preliminary study analysis under the direction of the Principal Investigator or senior ... IRB. * Ensures consent process is performed and documented in compliance with regulations and ...
Contractual Irb Analyst information
What are the key skills and qualifications needed to thrive as a Contractual IRB Analyst, and why are they important?
What is the difference between Contractual Irb Analyst vs Clinical Research Coordinator?
| Aspect | Contractual Irb Analyst | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's degree, IRB-related certifications | Bachelor's degree, clinical research training |
| Work Environment | IRB offices, regulatory agencies | Research sites, hospitals, clinics |
| Employer & Industry | Research institutions, biotech companies | Hospitals, research centers |
| Job Focus | IRB review, compliance, regulatory documentation | Participant recruitment, study coordination |
The Contractual Irb Analyst primarily focuses on IRB review and regulatory compliance, working closely with research protocols and ethics boards. In contrast, a Clinical Research Coordinator manages participant recruitment and day-to-day study activities. Both roles require knowledge of clinical research processes but differ in their specific responsibilities and work environments.
What are Contractual IRB Analysts?
What are some common challenges a Contractual IRB Analyst might face when working with diverse research protocols?
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Full-time
Medical, Retirement, PTO
Posted 10 days ago
University Of Chicago rating
8.1
Based on 47 frontline employees who took The Breakroom Quiz
152nd of 612 rated colleges and universities
Job description
Department
BSD OCR - Research Compliance
About the Department
Job Summary
The Clinical Research Financial Analyst is an integral member of the Office of Clinical Research. Under the direction of the Associate Director Research Billing Compliance, the Clinical Research Financial Analyst will promote and facilitate a culture of financial compliance through the regulatory and financial amendments to clinical research studies to ensure institutional adherence with Federal, State, and Local Regulations and Guidelines.
Activities include but are not limited to supporting research revenue cycle management through research billing review, processing payments, reviewing and preparing research billing documentation, and producing research financial reporting, as well as department projects and initiatives to support research billing compliance tasks as needed.
Responsibilities
Perform all research billing activities including, but not limited to: daily charge review, billing issue resolution, reconciliation and payment of research accounts.
Conduct research billing quality assurance activities, such as individual patient billing audits, study audits, device audits and validation of data and information contained within institutional systems (e.g. Epic, IRB system, clinical trial management system, etc.).
Assist in the development and design of training and resource materials related to research billing and financial management in collaboration with others in the office.
Follow standard operating procedures and policies to ensure compliant research billing as mandated by regulatory agencies (FDA, OHRP, OIG, CMS).
Has a moderate/solid understanding of coding procedures, workflow issues, billing infrastructure, and performance of Clinical Revenue staff.
Generates Epic and CTMS reports for analysis, monitoring and improving research billing metrics and processes.
Effectively collaborates with Clinical Trial Financial Group, Hospital Revenue Cycle team, study teams, research subjects, IRB, and other stakeholders to address research billing challenges.
Ensure institutional research billing compliance with Medicare's Clinical Trial Policy, federal regulations, and contractual agreements.
Maintain an understanding of Medicare's Clinical Trial Policy (NCD 310.1) and related guidance documents.
Assist in developing and maintaining polices, SOPs & SOWs related to clinical research billing process.
Stays current on all internal processes related to research billing, Medicare, National and local, regulations and guidelines, policies and procedures governing Research billing.
Prioritizes chart documentation and maintaining requirements within the department. Ensures all processes involved in accurately posting professional fees.
Has a moderate/solid understanding of coding procedures, workflow issues, billing infrastructure, and performance of Clinical Revenue staff. Informs department administrators, physicians, and Coder/Abstractors of regulatory changes.
Participates and may lead in training sessions, performing audits, and promoting an understanding of procedures, policies, and expectations in promotion of compliance efforts.
Performs other related work as needed.
Minimum Qualifications
Education:
Minimum requirements include a college or university degree in related field.
Work Experience:
Certifications:
---
Preferred Qualifications
Education:
Bachelor's degree in finance, accounting, business administration, or health information management.
Experience:
2-4 years' experience with healthcare clinical research billing preferably in academic medical setting, clinical research management, health system operations.
Experience with Epic Research Billing functions.
Experience with a Clinical Trial Management system (CTMS) preferably OnCore, financial software, ERP systems.
Accounting and finance experience strongly preferred.
Preferred Competencies
Knowledge of the Medicare Clinical Trials Policy and other federal, state and institutional clinical research regulations.
Expertise in CPT, Modifiers, ICD, and HCPCS codes to support billing and compliance efforts.
Strong knowledge of clinical trial contracting, revenue recognition principles, and relevant regulatory guidelines (e.g., ICH-GCP).
Excellent attention to detail and analytical skills, with a focus on accuracy in financial operations.
Strong communication and interpersonal skills for effective collaboration with cross-functional teams and external partners.
Expertise in Microsoft Excel.
Excellent Written and verbal communication skills.
Strong investigative and problem-solving skills.
Working Conditions
Office environment.
Application Documents
Resume (required)
Cover Letter (required)
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) MUSTbe uploaded via the My Experience page, in the section titled Application Documents of the application.
Job Family
Role Impact
Scheduled Weekly Hours
Drug Test Required
Health Screen Required
Motor Vehicle Record Inquiry Required
Pay Rate Type
FLSA Status
Pay Range
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
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.
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:http://securityreport.uchicago.edu.Paper copies of the Report are available, upon request, from the University of Chicago Police Department, 850 E. 61st Street, Chicago, IL 60637.
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Company size
10,000+ Employees
Headquarters location
Chicago, IL, US
Year founded
1890