1

Oncore Jobs in Florida (NOW HIRING)

Oversees the use of Electronic Data Capture (EDC) systems and OnCore CTMS, as necessary for operations. Manages the development of standard operating procedures (SOPs) for data quality assurance.

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 ...

Lab Supervisor

Gainesville, FL · On-site

$68K - $78K/yr

Familiarity with CTMS/OnCore and Epic systems. * Advanced Excel and data management skills. * Experience preparing for and supporting inspections/audits Special Instructions to Applicants: The ...

Completes OnCore worksheet to ensure proper protocol billing. * Performs the informed consent process following GCP. * Performs other duties as assigned. Annual Salary Range: $60,835 - $98,855 ...

Lab Supervisor

Gainesville, FL · On-site

$68K - $78K/yr

Familiarity with CTMS/OnCore and Epic systems. * Advanced Excel and data management skills. * Experience preparing for and supporting inspections/audits Special Instructions to Applicants: The ...

Showing results 21-30

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 Coordinator I-Department of Neurosurgery (Spine)

University of Florida

Gainesville, FL • On-site

$53K - $60K/yr

Full-time

Posted 5 days ago


University Of Florida rating

7.2

Company rating: 7.2 out of 10

Based on 108 frontline employees who took The Breakroom Quiz

385th of 621 rated colleges and universities


Job description

Clinical Research Coordinator I-Department of Neurosurgery (Spine)
Job no: 540820
Work type: Staff Full-Time
Location: Main Campus (Gainesville, FL)
Categories: Grant or Research Administration
Department:29190000 - MD-NEUROLOGICAL SURGERY
Classification Title:
Clinical Research Coordinator I
Classification Minimum Requirements:
Associate's degree or an allied health professional degree in an appropriate area and one year of relevant experience; or an equivalent combination of education and experience.
Job Description:
Research Coordination and Study Support
  • Support the conduct of clinical research studies and clinical trials in compliance with approved protocols, Good Clinical Practice (GCP), institutional policies, and applicable regulatory requirements.
  • Screen potential research participants and assist with patient recruitment and enrollment activities.
  • Participate in the informed consent process and assist with educating participants and families regarding study procedures, requirements, interventions, and follow-up activities.
  • Coordinate protocol-related study visits, research procedures, and participant follow-up activities.
  • Schedule participant visits, testing, and study-related procedures.
  • Maintain accurate and complete study source documentation and research records.
  • Perform data collection and accurate data entry into study databases, case report forms (CRFs), and electronic data capture systems.
  • Assist with the resolution of data queries and routine data quality review activities.
  • Collect, process, and ship laboratory specimens as required by study protocols.
  • Support participant safety by identifying and reporting adverse events and protocol deviations in accordance with study and institutional requirements.
  • Assist with study monitoring visits, audits, site initiation activities, and study closeout procedures.
  • Maintain essential regulatory documents and assist with the preparation and submission of regulatory materials to the Institutional Review Board (IRB) and other oversight bodies.
  • Assist with study registration and maintenance activities in ClinicalTrials.gov as assigned.
  • Retain and archive study records in accordance with institutional and sponsor requirements.
  • Participate in promoting Human Subjects Protection and ethical conduct of research activities.

Clinical Outcomes Data Collection and Management
  • Serve as a primary coordinator for collection of patient-reported outcome measures (PROMs) and other clinical outcomes data for Spine Program research studies and quality initiatives.
  • Administer, track, and manage PROM collection throughout the patient care continuum, including preoperative and postoperative follow-up periods.
  • Monitor completion rates and conduct participant outreach to improve data collection and retention.
  • Maintain outcomes databases and ensure accuracy, completeness, and integrity of collected data.
  • Assist with tracking clinical outcomes and quality metrics for Spine Program research projects and programmatic initiatives.
  • Generate routine reports and summaries of study enrollment, follow-up status, and outcomes data.
  • Support development and maintenance of data collection tools, dashboards, and reporting processes used for research and quality improvement initiatives.
  • Collaborate with clinical staff, providers, and research personnel to facilitate efficient collection and management of outcomes data.

Administrative and Program Support
  • Support Spine Research Program leadership and research staff with study-related administrative activities and special projects.
  • Coordinate research team meetings and assist with preparation of meeting materials and documentation.
  • Assist with preparation of reports, presentations, abstracts, manuscripts, and program-related documents.
  • Support management of study files, investigator documentation, and research program records.
  • Assist with study finance tracking and other operational activities as assigned.
  • Provide support for student, volunteer, and observer activities within the research program as appropriate.

Expected Salary:
$53,250-$60,500
Required Qualifications:
Associate's degree or an allied health professional degree in an appropriate area and one year of relevant experience; or an equivalent combination of education and experience.
Preferred:
-Experience working in a clinical setting or research setting.
-Familiar with medical terminology.
-Experience with systems, including Epic and OnCore.
-Familiar with GCP (Good Clinical Practice).
Special Instructions to Applicants:
For consideration, please complete an application and include a cover letter, resume and the names and email addresses of three to five references.
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
Health Assessment Required:Yes
Advertised: 17 Aug 2026 Eastern Daylight Time
Applications close: 28 Aug 2026 Eastern Daylight Time
Whatsapp Facebook LinkedIn Email App

What University Of Florida employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


University of Florida logo

About University of Florida

Sourced by ZipRecruiter

The University of Florida is one of the top ranked public universities in the United States (ranked top 5 amongst public universities in 2023 US news and world report). It is one of only a few comprehensive universities, having medical, veterinary, dental, nursing, public health, and engineering disciplines all co-localized on the same, contiguous campus to facilitate interdisciplinary collaboration. Gainesville is located in the northern region of Florida, within 1-1.5 hours of each coast, and just 1.5-2 hours to Orlando and Tampa. It is a small to medium-sized city with a low cost of living, excellent public and private schools, and southern hospitality. While Gainesville is widely recognized as the home of the Gators, it is quickly becoming known as a center for innovation and a place with a lifestyle that's comfortable for families, yet attractive for young professionals.

Industry

Colleges, universities, and professional schools

Company size

5,001 - 10,000 Employees

Headquarters location

Gainesville, FL, US

Year founded

1853