Maintains accurate accounts receivable and payable data in OnCore CTMS and VETS (Visit Earnings ... Works with other administrators on the procurement process including purchasing, internal ...
Maintains accurate accounts receivable and payable data in OnCore CTMS and VETS (Visit Earnings ... Works with other administrators on the procurement process including purchasing, internal ...
Working knowledge of OnCore, EPIC, and/or Oracle. * Clinical research certification (SoCRA, ACRP). Why apply to OHSU? We are Oregon's only public academic health center. In addition to caring for ...
Working knowledge of OnCore, EPIC, and/or Oracle. * Clinical research certification (SoCRA, ACRP). Why apply to OHSU? We are Oregon's only public academic health center. In addition to caring for ...
Clinical Research Coordinator I-School of Medicine, Georgia CTSA
Atlanta, GA · On-site
$23.50 - $31.50/hr
Or be a licensed as a practical nurse (LPN) and one year admin support or one year of licensed ... Experience with electronic medical records, REDCap, OnCore, eIRB, or other clinical research ...
Clinical Research Coordinator I-School of Medicine, Georgia CTSA
Atlanta, GA · On-site
$23.50 - $31.50/hr
Or be a licensed as a practical nurse (LPN) and one year admin support or one year of licensed ... Experience with electronic medical records, REDCap, OnCore, eIRB, or other clinical research ...
Working knowledge of OnCore, EPIC, and/or Oracle. * Clinical research certification (SoCRA, ACRP). We are Oregon's only public academic health center. In addition to caring for patients, we lead ...
Working knowledge of OnCore, EPIC, and/or Oracle. * Clinical research certification (SoCRA, ACRP). We are Oregon's only public academic health center. In addition to caring for patients, we lead ...
Working knowledge of OnCore, EPIC, and/or Oracle. * Clinical research certification (SoCRA, ACRP). Why apply to OHSU? We are Oregon's only public academic health center. In addition to caring for ...
Working knowledge of OnCore, EPIC, and/or Oracle. * Clinical research certification (SoCRA, ACRP). Why apply to OHSU? We are Oregon's only public academic health center. In addition to caring for ...
Working knowledge of OnCore, EPIC, and/or Oracle. * Clinical research certification (SoCRA, ACRP). Why apply to OHSU? We are Oregon's only public academic health center. In addition to caring for ...
Working knowledge of OnCore, EPIC, and/or Oracle. * Clinical research certification (SoCRA, ACRP). Why apply to OHSU? We are Oregon's only public academic health center. In addition to caring for ...
Or be a licensed as a practical nurse (LPN) and one year admin support or one year of licensed ... Experience with electronic medical records, REDCap, OnCore, eIRB, or other clinical research ...
Or be a licensed as a practical nurse (LPN) and one year admin support or one year of licensed ... Experience with electronic medical records, REDCap, OnCore, eIRB, or other clinical research ...
Clinical Research Supervisor 1 - Pediatrics
Los Angeles, CA · On-site
$86K - $184K/yr
Prior experience with a clinical research management system such as OnCore. Prior experience using ... administrators, work colleagues, representatives from sponsors and others to achieve maximum ...
Clinical Research Supervisor 1 - Pediatrics
Los Angeles, CA · On-site
$86K - $184K/yr
Prior experience with a clinical research management system such as OnCore. Prior experience using ... administrators, work colleagues, representatives from sponsors and others to achieve maximum ...
Clinical Research Coordinator I-School of Medicine, Georgia CTSA
Atlanta, GA · On-site
$23.50 - $31.50/hr
Or be a licensed as a practical nurse (LPN) and one year admin support or one year of licensed ... Experience with electronic medical records, REDCap, OnCore, eIRB, or other clinical research ...
Clinical Research Coordinator I-School of Medicine, Georgia CTSA
Atlanta, GA · On-site
$23.50 - $31.50/hr
Or be a licensed as a practical nurse (LPN) and one year admin support or one year of licensed ... Experience with electronic medical records, REDCap, OnCore, eIRB, or other clinical research ...
Research Administrator 3 / Pediatrics Clinical Research Operations Manager
Portland, OR · On-site
$93K - $149K/yr
Working knowledge of OnCore, EPIC, and/or Oracle. * Clinical research certification (SoCRA, ACRP). Why apply to OHSU? We are Oregon's only public academic health center. In addition to caring for ...
Research Administrator 3 / Pediatrics Clinical Research Operations Manager
Portland, OR · On-site
$93K - $149K/yr
Working knowledge of OnCore, EPIC, and/or Oracle. * Clinical research certification (SoCRA, ACRP). Why apply to OHSU? We are Oregon's only public academic health center. In addition to caring for ...
Rsch Pro 2-Rsch Coord-Gnrlst
Minneapolis, MN · On-site
$55K - $75K/mo
Administer surveys to and conduct interviews with study participants * Maintain high quality source ... Experience with REDCap data management and Oncore Clinical Trials Management System * Bilingual ...
Rsch Pro 2-Rsch Coord-Gnrlst
Minneapolis, MN · On-site
$55K - $75K/mo
Administer surveys to and conduct interviews with study participants * Maintain high quality source ... Experience with REDCap data management and Oncore Clinical Trials Management System * Bilingual ...
IT Training Specialist
Indianapolis, IN · On-site
Assists application administrators in enforcing data entry requirements General Responsibilities ... Experience working in or supporting a clinical research management system, specifically OnCore
IT Training Specialist
Indianapolis, IN · On-site
Assists application administrators in enforcing data entry requirements General Responsibilities ... Experience working in or supporting a clinical research management system, specifically OnCore
Coordinator, Clinical Studies - Lymphoma-Myeloma
$34.62 - $41.59/hr
... electronically Administer validated patient-reported outcome tools according to protocol ... including OnCore) Enter study data accurately and in a timely manner and verify data quality ...
Coordinator, Clinical Studies - Lymphoma-Myeloma
$34.62 - $41.59/hr
... electronically Administer validated patient-reported outcome tools according to protocol ... including OnCore) Enter study data accurately and in a timely manner and verify data quality ...
Clinical Research Coordinator III, Various Departments
Cincinnati, OH · On-site
$56K - $62K/yr
Primary Location Burnet Campus Department Pediatrics / CCRF Admin Shift Day (United States of ... OnCore, or similar) • Specimen processing and biobanking • Healthcare, patient-facing, or ...
Clinical Research Coordinator III, Various Departments
Cincinnati, OH · On-site
$56K - $62K/yr
Primary Location Burnet Campus Department Pediatrics / CCRF Admin Shift Day (United States of ... OnCore, or similar) • Specimen processing and biobanking • Healthcare, patient-facing, or ...
Familiarity with OnCore, EDC systems, EMRs, and clinical trial documentation * Knowledge of FDA ... It is unlawful in Massachusetts to require or administer a lie detector test as a condition of ...
Quick apply
Familiarity with OnCore, EDC systems, EMRs, and clinical trial documentation * Knowledge of FDA ... It is unlawful in Massachusetts to require or administer a lie detector test as a condition of ...
UNIV - Program Manager I - EP, Structural & Preventative Cardiology Clinical Trials - Department of
Charleston, SC · On-site
OnCore). * Provide guidance and support to division administrators and faculty regarding budgetary matters, including expense tracking, budget reallocation, and cost-saving opportunities. 10% - ...
UNIV - Program Manager I - EP, Structural & Preventative Cardiology Clinical Trials - Department of
Charleston, SC · On-site
OnCore). * Provide guidance and support to division administrators and faculty regarding budgetary matters, including expense tracking, budget reallocation, and cost-saving opportunities. 10% - ...
Coordinator, Clinical Studies - Lymphoma-Myeloma
Houston, TX · On-site
$57K/mo
... • Administer validated patient-reported outcome tools according to protocol requirements • ... OnCore) • Enter study data accurately and in a timely manner and verify data quality • Compile ...
Coordinator, Clinical Studies - Lymphoma-Myeloma
Houston, TX · On-site
$57K/mo
... • Administer validated patient-reported outcome tools according to protocol requirements • ... OnCore) • Enter study data accurately and in a timely manner and verify data quality • Compile ...
Human Subjects Research Coordinator II
Rochester, NY · On-site
$25.14 - $35.24/hr
Reviews study progress, including communicating with research administrator and updating OnCore or other workbooks on enrollment, visits, and other study procedures completed to ensure maximum ...
Human Subjects Research Coordinator II
Rochester, NY · On-site
$25.14 - $35.24/hr
Reviews study progress, including communicating with research administrator and updating OnCore or other workbooks on enrollment, visits, and other study procedures completed to ensure maximum ...
... OnCore) and play a decision-making role in any future related implementations. In collaboration with OCT, Offices of Compliance and Grants Management and the team of contract administrators within ...
... OnCore) and play a decision-making role in any future related implementations. In collaboration with OCT, Offices of Compliance and Grants Management and the team of contract administrators within ...
Human Subject Research Program/Project Support Coordinator II
Columbia, MO · On-site
$23 - $26/hr
... OnCore, and shared data platforms. • Analyze project information, timelines, budgets, and ... with administrators, faculty, staff, sponsors, and external partners to support research ...
Human Subject Research Program/Project Support Coordinator II
Columbia, MO · On-site
$23 - $26/hr
... OnCore, and shared data platforms. • Analyze project information, timelines, budgets, and ... with administrators, faculty, staff, sponsors, and external partners to support research ...
Oncore Administrator information
What is the difference between Oncore Administrator vs Clinical Trial Coordinator?
| Aspect | Oncore Administrator | Clinical Trial Coordinator |
|---|---|---|
| Credentials | Typically requires a degree in life sciences or healthcare, with certifications in clinical data management or EDC systems | Usually holds a degree in health sciences, nursing, or related fields; certifications in clinical research are common |
| Work Environment | Works primarily in clinical research settings, managing EDC systems like Oncore | Works in clinical sites or research offices, coordinating trial activities and patient enrollment |
| Employer & Industry | Pharmaceutical companies, CROs, academic research institutions | Hospitals, research sites, pharmaceutical companies |
The Oncore Administrator focuses on managing the Oncore electronic data capture system, ensuring data accuracy and compliance. In contrast, the Clinical Trial Coordinator handles day-to-day trial operations, patient coordination, and site management. Both roles are essential in clinical research but differ in their primary responsibilities and focus areas.
What are the key skills and qualifications needed to thrive as an Oncore Administrator, and why are they important?
What is an Oncore Administrator?
What are some common challenges Oncore Administrators face when managing clinical trial data, and how can they address them?

Full-time
Medical, Retirement, PTO
Posted 29 days ago
University Of Chicago rating
8.1
Based on 47 frontline employees who took The Breakroom Quiz
158th of 617 rated colleges and universities
Job description
Department
BSD OCR- Post Award
About the Department
The mission of the Office of Clinical Research is to catalyze clinical research by providing expertise, resources, infrastructure, and systems that facilitate clinical research operations and enable collaboration across the enterprise while promoting compliance and human subject protection on behalf of our diverse community of patients and volunteers. Together, we elevate the human experience with knowledge and health care.
Job Summary
The Clinical Trial Financial Manager provides administrative support in an intensive customer service environment for the Clinical Trial Financial Group CTFG within the Office of Clinical Research for the Biological Sciences Division.
Responsibilities
Serves as a primary account administrator for clinical research study accounts.
Creates accounts and works within the financial accounting system, Oracle.
Allocates, authorizes, monitors, and controls expenses on clinical research study accounts.
Manages check and wire-transfer deposits and earnings invoicing for industry-funded clinical trials.
Maintains accurate accounts receivable and payable data in OnCore CTMS and VETS (Visit Earnings Tracking System).
Facilitates timely reconciliation and close-out of terminated clinical trial financial accounts.
Maintains, oversees, reconciles, and corrects errors in accounts. Processes clinical research and core bills for payment.
Partners with CT Contracts Managers on budgetary amendment implementation.
Communicates regularly with study staff on accrual tracking and provides training in study financial management.
Works with other administrators on the procurement process including purchasing, internal requisitioning, and personal and travel reimbursements.
Partner with grants administrators to manage financial and administrative aspects
Project proposal preparation, submission, and post-award grant administration.
Advises and assists in relationship management and communications with funding agencies, subcontractors, and others.
Monitors expenditures on approximately 560 - 700 active individual faculty accounts.
Proposes solutions to discovered problems and fixes according to proper policy and compares actual spending to original budget and identifies any variances with the particular attention being paid to faculty salary.
Develops a working knowledge of University policies and procedures as well as a working knowledge of policies and procedures of various funding agencies.
Creates and maintains excel spreadsheets and databases to track Division's clinical research.
Works closely with Section Administrators and Department Leadership to effectively manage faculty clinical research accounts and ensure proper spending.
Seeks new avenues for funding and grant opportunities and ensures that notices of relevant opportunities are brought to faculty attention. Works with sponsors to draft proposal budgets in accordance with University needs, with a moderate level of guidance and direction.
Handles straightforward post-award activities including account creations, regulatory and compliance monitoring, salary allocations, effort reporting, grant projections, cost allocations, cost center charges, equipment inventory, invoice preparation, grant closing process, and account closing.
Prepares summaries of grants and effort allocations for Principal Investigators, meets with them and responds to their questions. Coordinates with other departments/units/divisions regarding multi investigator grants. Serves as department contact for annual audits and agency site visits.
Performs other related work as assigned.
Minimum Qualifications
Education:
Minimum requirements include a college or university degree in related field.
Work Experience:
Certifications:
---
Preferred Qualifications
Education:
Bachelor's degree.
Experience:
Working knowledge in Oracle, Business Objects, and academic medical operations.
An understanding of fund accounting principles, federal and major non-federal post-award policies, allowable cost policies, and fundamental academic policies, allowable cost policies, and fundamental academic medical research accounting.
Preferred Competencies
Strong computer skills including word processing, database management, and spreadsheet skills.
Excellent verbal and written communication skills.
Attention to detail.
Flexible and adaptable.
Knowledge of general accounting standards and auditing.
Strong organizational skills.
Sound financial and analytic skills.
Research issues and propose solutions to problems.
Demonstrated initiative in improving processes and enhancing systems.
Exercise sound judgment, discretion and tact.
Exceptional time management skills and the ability to handle multiple, concurrent tasks within deadlines.
Work with individuals from across the division and University.
Proficient in research methods and funding sources.
Expertise with clinical trials.
Background with federal and non-federal regulations for grant management.
Proficiency with fund accounting.
Familiarity with federal and non-federal grant and contract policies
Working Conditions
Office environment.
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) 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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About University of Chicago
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Industry
Colleges, universities, and professional schools
Company size
10,000+ Employees
Headquarters location
Chicago, IL, US
Year founded
1890