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Oncore Jobs in Florida (NOW HIRING)

The position is responsible for administrative and financial oversight of departmental-sponsored research, as well as OnCore report analysis and junior clinical research staff training. General ...

Experience with Clinical Trial Management Systems (CTMS), such as OnCore. Experience with Electronic Data Capture (EDC) systems Quality assurance, auditing, and regulatory compliance oversight.

To process and analyze reports in OnCore, as needed. Key Duties & Responsibilities * Acts as a resource for faculty and staff regarding administrative duties for industry and sponsored clinical ...

Enters protocol specific data into required institutional systems (IRAP and OnCore). * Maintains Delegation of Authority logs. * Performs other duties as assigned. Hourly Range : $18.85 - $30.65 High ...

Study Data Management - Utilizing REDCap and OnCore, performs study data input, monitoring, and quality control for ongoing clinical research programs. Ensures study participant consent, HIPAA ...

... OnCore). 6. Serves as liaison between faculty, the Office of Sponsored Programs, IRB, other university offices, and external collaborators to facilitate communication, resolve issues, and ensure ...

Conducts periodic internal audits of fields in the OnCore CTMS to ensure compliance with institutional requirements. Develops reports and assists unit leadership as needed. Develops standard ...

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Oncore information

What is an Oncore?

An Oncore job typically refers to a position within the Oncore platform, a workforce management system used for contingent labor and project-based work. These jobs can vary across industries and may include contract, temporary, or gig-based roles. Oncore helps businesses efficiently manage and pay their contingent workforce while ensuring compliance with labor regulations. If you are hired for an Oncore job, you may work as an independent contractor or temporary employee depending on the arrangement.

What does an Oncore Clinical Research Associate do?

A typical day for an Oncore Clinical Research Associate involves monitoring ongoing clinical trials, ensuring they are conducted according to protocol, and reviewing data for accuracy and compliance. You'll frequently interact with study site staff, coordinate with investigators, and document findings in clinical trial management systems like OnCore. The role may also include onsite visits, remote monitoring, and regular meetings with sponsors or regulatory teams. Timely communication and attention to protocol details are crucial, making it a dynamic and collaborative work environment with opportunities to learn and grow within the clinical research field.

What are the key skills and qualifications needed to thrive in the Oncore position?

To thrive in an Oncore Clinical Research Associate role, a background in life sciences, clinical trial monitoring experience, and knowledge of regulatory guidelines such as GCP are essential. Proficiency in electronic data capture (EDC) systems, trial management software, and certifications like ACRP or SOCRA are often required. Excellent organizational skills, attention to detail, and effective communication help candidates excel in multi-site coordination and team settings. These capabilities ensure the smooth execution, compliance, and high-quality outcomes of clinical research studies.

Infographic showing various Oncore job openings in Florida as of August 2026, with employment types broken down into 91% Full Time, 6% Part Time, and 3% Contract. Highlights an 84% In-person, 6% Hybrid, and 10% Remote job distribution.

CLINICAL RESEARCH ADMINISTRATOR III

UAB

Tampa, FL

$55K - $89K/yr

Full-time

Re-posted 28 days ago


UAB Medicine rating

7.3

Company rating: 7.3 out of 10

Based on 190 frontline employees who took The Breakroom Quiz

306th of 891 rated healthcare providers


Job description

The University of Alabama at Birmingham (UAB), Neurology Chair Office, is seeking a Clinical Research Administrator III in the central Neurology Research Unit. The position is responsible for administrative and financial oversight of departmental-sponsored research, as well as OnCore report analysis and junior clinical research staff training.

General Responsibilities

  • To act as a resource for faculty and staff regarding administrative duties for industry and sponsored clinical research.

  • To serve as an informational and referral resource for the clinical research community.

  • To work with necessary parties to identify compliance, legal, IP and business/financial risk.

  • To manage accounts across all studies as needed.

  • To process and analyze reports in OnCore, as needed.

Key Duties & Responsibilities

  1. Management and oversight of departmental-sponsored research accounts.

  2. OnCore report analysis/research activity data analysis.

  3. Advises PIs/study personnel on budgetary parameters and operational requirements of clinical studies.

  4. Clinical trial account reconciliation and post-award management.

  5. Performs other duties as assigned.

Annual Salary Range:   $55,180 - $89,670

Bachelor's degree in a related field and five (5) years of related experience required. Work experience may NOT substitute for education requirement. Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification preferred.
 

UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.


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