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Oncore Analyst Jobs (NOW HIRING)

Financial Analyst I OCR

Charlotte, NC · On-site +1

$28.55 - $42.85/hr

The Clinical Research Financial Analyst I is a position that resides in the Office of Clinical ... Systems Support 1. Primary user of OnCore; use of EPIC as necessary. General Support 1. Prioritizes ...

Test Engineer III

Longmont, CO · On-site

$80K - $100K/yr

Sustaining engineering and Tester capacity analysis, manufacturing failure data analysis and improvement plan presentations. * Support and follow all ISO standards related to OnCore's various Quality ...

Test Engineer I (24522)

Chatsworth, CA · On-site

$75K - $85K/yr

Sustaining engineering and Tester capacity analysis, manufacturing failure data analysis and improvement plan presentations. * Support and follow all ISO standards related to OnCore's various Quality ...

Sustaining engineering and Tester capacity analysis, manufacturing failure data analysis and improvement plan presentations. * Support and follow all ISO standards related to OnCore's various Quality ...

Sustaining engineering and Tester capacity analysis, manufacturing failure data analysis and improvement plan presentations. * Support and follow all ISO standards related to OnCore's various Quality ...

Sustaining engineering and Tester capacity analysis, manufacturing failure data analysis and improvement plan presentations. * Support and follow all ISO standards related to OnCore's various Quality ...

Test Engineer III (24046)

Longmont, CO · On-site

$80K - $100K/yr

Sustaining engineering and Tester capacity analysis, manufacturing failure data analysis and improvement plan presentations. * Support and follow all ISO standards related to OnCore's various Quality ...

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Oncore Analyst information

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$35K

$75.6K

$132K

How much do oncore analyst jobs pay per year?

As of Jun 11, 2026, the average yearly pay for oncore analyst in the United States is $75,606.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,000.00 and $91,500.00 per year, depending on experience, location, and employer.

What is an Oncore Analyst?

An Oncore Analyst is a professional who specializes in managing and supporting the OnCore Clinical Trial Management System (CTMS), a software tool commonly used by research organizations and academic medical centers. They are responsible for data entry, process optimization, user training, and ensuring regulatory compliance within the OnCore platform. Oncore Analysts help streamline clinical trial operations by maintaining accurate study records, generating reports, and providing technical support to research staff. Their role is crucial in improving the efficiency and integrity of clinical research management.

What is the difference between Oncore Analyst vs Clinical Data Coordinator?

AspectOncore AnalystClinical Data Coordinator
CredentialsBachelor's degree in life sciences or related field; experience with clinical trial data systemsBachelor's degree; experience in data management and clinical trial processes
Work EnvironmentPharmaceutical or biotech companies, clinical research organizationsHospitals, research institutions, clinical trial sites
Industry UsageUsed for managing and analyzing clinical trial data within Oncore softwareOversees data collection, entry, and quality control in clinical trials

The Oncore Analyst primarily focuses on managing and analyzing clinical trial data within the Oncore system, ensuring data accuracy and compliance. In contrast, the Clinical Data Coordinator handles data collection, entry, and quality control at clinical trial sites. Both roles require similar educational backgrounds and work in related environments, but their responsibilities differ in scope and focus.

How does an Oncore Analyst typically collaborate with clinical research teams during a project's lifecycle?

Oncore Analysts work closely with clinical research coordinators, principal investigators, and regulatory specialists to ensure accurate study setup, data management, and compliance within the Oncore Clinical Trials Management System. Throughout a project's lifecycle, analysts provide technical support, train staff on system updates, and troubleshoot data or workflow issues. This collaborative environment requires strong communication skills and a proactive approach to problem-solving, as Oncore Analysts often act as a bridge between IT and research operations to streamline processes and maintain data integrity.

What are the key skills and qualifications needed to thrive as an Oncore Analyst, and why are they important?

To thrive as an Oncore Analyst, you need strong analytical skills, experience with clinical trial management, and a relevant degree such as in healthcare, information systems, or a related field. Proficiency with the OnCore Clinical Trial Management System (CTMS), electronic data capture tools, and often certifications in clinical research or data management are typically required. Excellent problem-solving abilities, attention to detail, and effective communication skills help an Oncore Analyst collaborate with research teams and ensure data integrity. These skills are vital to support efficient clinical trial operations, maintain compliance, and drive successful research outcomes.
More about Oncore Analyst jobs
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What states have the most Oncore Analyst jobs? States with the most job openings for Oncore Analyst jobs include:

Project Specialist- Administrative

USC Gould School of Law

Los Angeles, CA • On-site, Remote

$30.14 - $38.71/hr

Full-time

Posted 5 days ago


Job description

OnCore CTMS Clinical Research Calendar Builder

USC Clinical Trials Office is seeking a Clinical Trial Management System (OnCore) Calendar Builder. Working directly under the supervision of the CTMS Manager, the Calendar Builder works directly with research teams and central offices and requires an in-depth understanding of clinical research to successfully manage their duties.

The successful candidate will be motivated, proactive, resourceful, and detail oriented. The position requires excellent organizational and communication skills with the ability to be decisive and adaptable. This position will build and configure study calendars in OnCore based on provided study documents. Candidate will be responsible for interpreting research protocols, managing competing priorities, and providing superior customer service.

Required Qualifications: Bachelor's degree in clinical research, Science, Health Sciences, Information Technology, Business or related field or full-time professional experience in a clinical research setting and/or experience working with applications/information systems in a healthcare, finance, or other highly regulated environment.

Preferred Qualifications:

  • One-year experience working with web-based applications/information systems in a healthcare, finance, or other highly regulated environment.

  • Prior experience in building calendars within OnCore at an academic medical center is preferred.

  • Knowledge of cancer research, the oncology field, or related experience.

  • Experience with other CTMS or financial data systems in support of clinical research is desirable.

  • Experience providing technical support to customers.

  • Project management experience.

Essential job duties include, but are not limited to:

  • Build and configure study calendars based on documents submitted for clinical trial data capture in accordance with the terms of the protocol in OnCore.

  • Conduct kick-off meetings with study team, coverage analyst and budget specialists regarding calendar design.

  • Perform system testing as directed and quality control of application functionality during application upgrades.

  • Assist coverage analysts, budget specialists and cancer center employees who encounter technical issues, problems or have questions relating to OnCore.

  • Collaborate with direct supervisor, finance team, clinical research team, project manager, health system representatives, consultants and vendors to ensure overall completion of goals, schedules, and deadlines.

  • Stay up to date on all new and evolving institutional changes as they relate to policy, pricing, budgeting, etc. for clinical trial data captured in OnCore.

  • Provide ad hoc reporting to OnCore, Clinical Trials Office and Cancer Center leadership, as necessary.

  • Assist the OnCore support team in developing learning tools as they relate to calendar and OnCore in general.

  • Act as a resource to other staff utilizing OnCore.

  • Perform other duties as assigned.

Follows established USC and department policies, procedures, objectives, performance improvement, attendance, safety, environmental, and infection control guidelines, including adherence to the workplace Code of Conduct and Compliance Plan.

This position is fully remote. Work hours may be subject to change depending on business needs.

The hourly rate range for this position is $30.14 - $38.71. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations

Minimum Education: Bachelor's degree
Addtional Education Requirements Combined experience/education as substitute for minimum education
Minimum Experience: 2 years
Minimum Skills: Directly related project or administrative experience.
Preferred Education: Master's degree
Preferred Experience: 3 years

USC is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other characteristic protected by law or USC policy. USC observes affirmative action obligations consistent with state and federal law. USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to theBackground Screening Policy Appendix Dfor specific employment screen implications for the position for which you are applying.

We provide reasonable accommodations to applicants and employees with disabilities. Applicants with questions about access or requiring a reasonable accommodation for any part of the application or hiring process should contact USC Human Resources by phone at (213) 821-8100, or by email atuschr@usc.edu. Inquiries will be treated as confidential to the extent permitted by law.

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If you are a current USC employee, please apply to this  USC job posting in Workday by copying and pasting this link into your browser:

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