
Research Coordinator I/II/III - Oncology
Weston, FL · HybridFull-time$48–72K/yrSeen 1 day agoSeen in employer's feed 1 day ago
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At a glance
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Job overview
The Research Coordinator for the Weston Cancer Research Group coordinates compliant human-subject research projects and supports clinical trials through study start-up, administrative work, and patient visits. The role includes protocol coordination, regulatory documentation, recruitment, informed consent, and audit preparation. The position works days from 8:00 a.m. to 5:00 p.m. and transitions to a hybrid schedule after six months, with one work-from-home day per week depending on business needs.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Join the Cleveland Clinic Florida's Weston Family Health Center and become a part of one of the most respected healthcare organizations in the world. Weston Family Health Center provides the communities in and around Weston with top-quality preventative health care, management of chronic conditions, and more.
As a Research Coordinator for the Weston Cancer Research Group, you will coordinate the compliant implementation and conduct of human subject research projects of medium workload and complexity. In this role, you will support clinical trials through study start-up, administrative activities and patient visits, with each day offering new opportunities to contribute to cancer research. Your work will help provide patients with access to potential new treatment options when standard options may be limited.
A caregiver in this role works days from 8:00 a.m. - 5:00 p.m.
After six months, this position transitions to a hybrid schedule, with the option to work from home one day per week, depending on business needs.
A caregiver who excels in this role will:
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Coordinates the implementation and conduct of research projects ensuring adherence to research protocol requirements including: timely completion and communication of regulatory documents, the development of data capture and monitoring plans, reporting of Serious Adverse Events as they occur and completion of Food and Drug Administration (FDA) and sponsor forms in accordance with GCP timelines.
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Serves as a liaison between investigators, research personnel, outside study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions.
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Collaborates with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols, including research subject recruitment.
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Monitors and reports project status.
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Completes regulatory documents, data capture and monitoring plans.
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Develops and maintains knowledge of research protocol to coordinate the comprehensive and compliant execution of assigned protocols.
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Assists with preparation for audits and response to audits.
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Maintains professional relationships, including frequent and open effective communication with internal and external
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constituents.
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Assists with the development of training and educational material for assigned research protocols.
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Provides and documents education as needed.
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Conducts and documents the informed consent process.
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Potentially assists with research project budget development.
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Other duties as assigned.
Minimum qualifications for a future caregiver include:
As a Research Coordinator I:
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High School Diploma or GED
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Two years of clinical research or healthcare experience required.
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An Associate or Bachelor's degree in health care or science related field may offset the experience requirement.
OR
As a Research Coordinator II
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High School Diploma or GED
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Three years of experience as a Research Coordinator I or performing the role of a Research Coordinator I
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An Associate or Bachelor's degree in health care or science related field may offset two years of experience requirement.
OR
As a Research Coordinator III
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High School Diploma or GED
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Five years of clinical research experience required.
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A Bachelor's degree in healthcare or science field may offset two years of clinical research experience requirement
Preferred qualifications for the ideal future caregiver include:
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Bachelor's degree in health care or science related field
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Oncology and/or research experience
Physical Requirements:
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Ability to perform work in a stationary position for extended periods
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Ability to operate a computer and other office equipment
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Ability to communicate and exchange accurate information
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In some locations, ability to move up to 25 pounds
Personal Protective Equipment:
- Follows standard precautions using personal protective equipment as required.
Pay Range
Minimum Annual Salary: $47,530.00
Maximum Annual Salary: $72,475.00
The pay range displayed on this job posting reflects the anticipated range for new hires. A successful candidate's actual compensation will be determined after taking factors into consideration such as the candidate's work history, experience, skill set and education. The pay range displayed does not include any applicable pay practices (e.g., shift differentials, overtime, etc.). The pay range does not include the value of Cleveland Clinic's benefits package (e.g., healthcare, dental and vision benefits, retirement savings account contributions, etc.).
Cleveland Clinic Health System is pleased to be an equal employment employer: Women / Minorities / Veterans / Individuals with Disabilities
How this job compares
Set against the 625 open Clinical Research Coordinator jobs on Olive Jobs, counted November 6, 2026.
- Pay
- This posting$48–72K/yr
- US median$56–74K/yr162 salary ranges
This range's midpoint, $60K, is 9% below the US median midpoint ($66K) — in the middle half of Clinical Research Coordinator salary ranges across the US.
- Openings
- Olive Jobs lists 53 open Clinical Research Coordinator jobs in Florida and 625 across the US. 2% of them nationwide are listed as remote or flexible.
- Hiring the most in Florida
- University of Miami38 open
- AdventHealth6 open
- Actalent3 open
- Experience
- This posting asks for at least 2 years of experience; Clinical Research Coordinator postings that state a minimum ask for 2 years at the median (411 postings).
- Education
- This posting asks for a high school diploma; 260 of the 625 open Clinical Research Coordinator jobs (42%) ask for a high school diploma or higher.
Counted across the open, public US postings on Olive Jobs on November 6, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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