Clinical Research Analyst I: CTMS & Protocols

University of Florida

Jacksonville (FL)

On-site

USD 53,000 - 60,000

Full time

10 hours ago
Be an early applicant

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

University of Florida’s Clinical Trials Management System (CTMS) team seeks a Clinical Research Analyst I to support protocol development, coverage analyses, and workflow management within the CTMS across the Jacksonville campus. The role collaborates with investigators, administrators, and study personnel to ensure compliance and efficient study execution.

The ideal candidate has a Bachelor's degree in a relevant field and one year of experience, with familiarity in CTMS systems and strong

Qualifications

  • Bachelor's degree in an appropriate area and one year of relevant experience or an equivalent combination of education and experience.
  • Familiarity with OnCore CTMS by Advarra or similar clinical trial management software preferred.
  • Background in clinical research administration or financial management is desirable.
  • Strong organization, communication, and documentation skills required.

Responsibilities

  • Support clinical trial operations and protocol management within the CTMS.
  • Assist with protocol coverage analyses and Medicare Coverage Analyses (MCAs).
  • Build and maintain billing grids and sponsor calendars in CTMS.
  • Provide guidance to study teams on CTMS and institutional processes.
  • Ensure data integrity, regulatory compliance, and timely task completion.

Skills

CTMS familiarity
Customer service
Organizational skills
Problem solving
Time management
Microsoft Office

Education

Bachelor's degree in an appropriate area

Tools

OnCore CTMS
Microsoft Office

Job description

University of Florida’s Clinical Trials Management System (CTMS) team seeks a Clinical Research Analyst I to support protocol development, coverage analyses, and workflow management within the CTMS across the Jacksonville campus. The role collaborates with investigators, administrators, and study personnel to ensure compliance and efficient study execution.

The ideal candidate has a Bachelor's degree in a relevant field and one year of experience, with familiarity in CTMS systems and strong

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Clinical Research Analyst I — CTMS & Protocol Operations
Clinical Research Analyst I — CTMS & Protocol Operations

University of Florida • Gainesville (FL)

On-site
USD 53,000 - 60,000
Clinical Trials Operations Analyst (CTMS)
Clinical Trials Operations Analyst (CTMS)

University of Florida College of Medicine - Jacksonville • Jacksonville (FL)

On-site
USD 53,000 - 60,000
Clinical Research Analyst I
Clinical Research Analyst I

University of Florida College of Medicine - Jacksonville • Jacksonville (FL)

On-site
USD 53,000 - 60,000
Clinical Research Analyst I
Clinical Research Analyst I

University of Florida • Jacksonville (FL)

On-site
USD 53,000 - 60,000
Clinical Research Analyst I
Clinical Research Analyst I

University of Florida • Gainesville (FL)

On-site
USD 53,000 - 60,000
Clinical Trials Research Associate
Clinical Trials Research Associate

University of Florida Jacksonville Physicians, Inc. • Jacksonville (FL)

On-site
USD 40,000 - 55,000
Remote CTMS Operations Analyst - Clinical Trials
Remote CTMS Operations Analyst - Clinical Trials

Total Renal Care • United States

Remote
USD 52,000 - 78,000
CTMS TECHNICAL ANALYST
CTMS TECHNICAL ANALYST

LSU • New Orleans (LA)

On-site
USD 65,000 - 90,000
Senior Oncology CTMS Analyst - Drive Clinical Trials
Senior Oncology CTMS Analyst - Drive Clinical Trials

Nicklaus Children's • Miami (FL)

On-site
USD 85,000 - 120,000
Senior Oncology CTMS Lead: Trials Data & Training
Senior Oncology CTMS Lead: Trials Data & Training

Nicklaus Children's • Miami (FL)

On-site
USD 60,000 - 80,000