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Oncore Analyst Jobs in Florida (NOW HIRING)

UAB

CLINICAL RESEARCH ADMINISTRATOR III

Tampa, FL · On-site

$55K - $89K/yr

To process and analyze reports in OnCore, as needed. Key Duties & Responsibilities * Management and oversight of departmental-sponsored research accounts. * OnCore report analysis/research activity ...

UAB

CLINICAL RESEARCH ADMINISTRATOR III (3)

Tampa, FL

$55K - $89K/yr

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 ...

UAB

PROGRAM DIRECTOR II

Tampa, FL · On-site

$60K - $98K/yr

... OnCore). 6. Serves as liaison between faculty, the Office of Sponsored Programs, IRB, other ... analytical, and problem-solving skills Ability to manage multiple complex projects simultaneously ...

All JobsOncore Analyst JobsOncore Analyst Jobs in Florida

Oncore Analyst information

See Florida salary details

$26.2K

$56.5K

$98.6K

How much do oncore analyst jobs pay per year?

As of Aug 14, 2026, the average yearly pay for oncore analyst in Florida is $56,500.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,400.00 and $68,400.00 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.

What are popular job titles related to Oncore Analyst jobs in Florida?

For Oncore Analyst jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Oncore Analyst jobs in Florida look for?

The top searched job categories for Oncore Analyst jobs in Florida are:

Oncore Analyst jobs near you
Infographic showing various Oncore Analyst job openings in Florida as of August 2026, with employment types broken down into 100% Full Time. Highlights an 52% In-person, and 48% Remote job distribution, with an average salary of $56,500 per year, or $27.2 per hour.

Sr. Oncore Analyst -Oncology - Remote (Full Time, Days)

Nicklaus Children's Health System

Miami, FL • On-site, Remote

$110K - $111K/yr

Full-time

Re-posted 28 days ago

Job description

Description
South Florida based position. We will also consider candidates that are willing to relocate.
Job Summary
The Senior Oncology CTMS Analyst will be responsible for the daily management/support of the Clinical Trials Management Software for the Nicklaus Children's Hospital Research Institute. Responsibilities include CTMS data entry, protocol/data updating, study calendar creation/development, budget shell creation/amending, data (metric/KPI) reporting, enrollment/screening dashboard updates, and collaboration with Research Institute Education on CTMS training/development. Serves as liaison to vendor partners and the Information Technology Department for shared system applications.
Job Specific Duties
  • Communicates research study progress reports (including PT screenings, enrollments, etc.) to relevant hospital units involved with research including the establishment of a good rapport with NCHS department leaders.
  • Responsible for the daily management/support (adds/edits/updates) of the Clinical Trials Management Software for the Nicklaus Children's Research Institute.
  • Responsible for RI Metric/KPI reporting of critical CTMS data to research administration and Nicklaus senior leadership.
  • Translates user requirements into functional and technical design specifications and reviews with client(s) to ensure accuracy.
  • Leads small to medium complexity for the RI suite of Cloud applications - upgrade, initiatives, or enhancements to workflows, including the design, build, and test phases.
  • Serves as a mentor/subject matter expert to internal and external clients and/or team members.
  • Assists and collaborates with the Research Institute Educator on CTMS training and development.
  • Creates budget shells/ financial schedules for new and existing (amended) study protocols.
  • Responsible for new study and study amendment protocol calendar creation in CTMS.
  • Assists with entering Research Patient information/data into CTMS within 72 hours of enrollment, patient visit or patient-related event.
  • Complies with the Research Finance Compliance policies and procedures including reporting requirements to research finance staff.
  • Utilizes Good Clinical Practices in the conduct of clinical trials as per established protocol.
  • Follows NCHS RI's Standard Operating Procedures, HIPAA, and FDA guidelines for clinical research, and keeps updated on those procedures and/or guidelines.
  • Collaborates with Research IT on research administrative-related software/system, updates, and purchases.
  • Assists department leadership in establishing application baselines, benchmarks, goals, objectives, and necessary resources to reach them .

Qualifications
Minimum Job Requirements
  • Bachelor's Degree in relevant field
  • 4 years of experience in research and healthcare data entry

Knowledge, Skills, and Abilities
  • Experience in pediatric clinical research in a hospital setting preferred.
  • Excellent communication skills in working with both children and adults.
  • Excellent organizational skills, detail-oriented, people-oriented, flexible, and adaptable to change.
  • Excellent time management skills.
  • Knowledge of research protocols and research study-related processes.
  • Software applications experience, including word processing, scheduling, and contact database, email, web browsing, hospital records, other database software, and office equipment.

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