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Oncore Clinical Jobs in California (NOW HIRING)

Program Specialist

Los Angeles, CA · On-site +1

$30.14 - $38/hr

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 ...

Program Specialist

Los Angeles, CA · On-site +1

$30.14 - $38/hr

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 ...

Clinical Research Coordinator Pay Rate Range: $35.00 - $70.00/hr (DOE, based on experience and ... Experience with Stanford systems (REDCap, eProtocol, OnCore, SeRA). * Knowledge of IRB processes ...

Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. * Ensure data accuracy, completeness ...

... and clinical research platforms (e.g., Epic, REDCap, Medidata, OnCore). * Must be knowledgeable in internet access to manage clinical trials case report forms. * Proficient with computerized and ...

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Oncore Clinical information

What is an Oncore Clinical professional?

Oncore Clinical professionals are specialists who work with the Oncore Clinical software platform, which is widely used for managing clinical trials and research studies in healthcare and academic settings. Their responsibilities often include configuring the system, supporting study teams, ensuring data integrity, and facilitating efficient workflow processes. They play a key role in streamlining clinical research operations and maintaining compliance with regulatory standards. Oncore Clinical professionals may work in roles such as system administrators, clinical research coordinators, or data managers.

What skills and qualifications are needed to thrive as an Oncore Clinical professional?

Success as an Oncore Clinical professional requires clinical research experience, knowledge of Good Clinical Practice (GCP), and a relevant degree in life sciences or healthcare. Familiarity with the OnCore Clinical Trial Management System (CTMS), electronic data capture platforms, and regulatory compliance tools is typically essential. Strong organizational skills, attention to detail, and effective communication help individuals excel in managing study protocols and collaborating with multidisciplinary teams. These competencies are vital to ensure efficient clinical trial operations, regulatory adherence, and high-quality research outcomes.

How does an Oncore Clinical professional typically collaborate with other departments in a healthcare organization?

Oncore Clinical professionals often work closely with multidisciplinary teams, including physicians, nurses, data managers, and regulatory specialists. Their responsibilities frequently involve coordinating patient care within oncology clinical trials, ensuring protocol adherence, and facilitating communication between research and clinical staff. Effective collaboration is crucial for maintaining compliance with regulatory guidelines and for the successful execution of clinical studies. Team meetings and regular updates are common practices to keep all stakeholders aligned and informed.

What is the difference between Oncore Clinical vs Clinical Research Coordinator?

AspectOncore ClinicalClinical Research Coordinator
CertificationsOften requires GCP training, clinical research certificationsTypically requires GCP training, sometimes certifications
Work EnvironmentPharmaceutical companies, clinical trial sites, research organizationsHospitals, research sites, academic institutions
Job ResponsibilitiesManaging clinical trial data, ensuring protocol compliance, using Oncore softwareParticipant recruitment, data collection, protocol adherence
Industry UsageUsed mainly in clinical trial management systemsCommonly employed in clinical trial coordination

Both roles involve clinical research but differ mainly in focus. Oncore Clinical professionals often manage trial data and use specific software, while Clinical Research Coordinators handle participant interactions and site operations. Understanding these differences helps in choosing the right career path or job search focus.

What are popular job titles related to Oncore Clinical jobs in California?

For Oncore Clinical jobs in California, the most frequently searched job titles are:

What job categories do people searching Oncore Clinical jobs in California look for?

The top searched job categories for Oncore Clinical jobs in California are:

What cities in California are hiring for Oncore Clinical jobs?

Cities in California with the most Oncore Clinical job openings:

Infographic showing various Oncore Clinical job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution.

Program Specialist

University of Southern California

Los Angeles, CA • On-site, Remote

$30.14 - $38/hr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.


University Of Southern California rating

8.4

Company rating: 8.4 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

102nd of 628 rated colleges and universities


Job description

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.

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.

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.

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 and employee must report to work at the USC Health Science Campus in Los Angeles, CA when scheduled. Work hours and remote days may be subject to change depending on business needs.

The hourly rate range for this position is $30.14 - $38.00. 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.

  • Notice of Non-discrimination
  • Employment Equity
  • Read USC's Clery Act Annual Security Report
  • USC is a smoke-free environment
  • Digital Accessibility

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:

https://wd5.myworkday.com/usc/d/inst/1$9925/9925$152207.htmld

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About University of Southern California

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The University of Southern California (USC) is not a conventional company, but a private research university established in the heart of Los Angeles, CA, US. Founded in 1880, it's one of the oldest private research universities in California. USC operates in the education industry providing primary services of higher education, research, and community development. This prestigious institution offers a comprehensive array of undergraduate, graduate, and professional programs across various disciplines, including the humanities, social sciences, and STEM (Science, Technology, Engineering, and Mathematics). The University is guided by its commitment to foster creativity, innovation, leadership, and discovery through academic excellence.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Los Angeles , CA, US

Year founded

1880