FULL-TIME
Posted Jul 5, 2026
Job Description
Location:The Sanctuary - Regional Cancer Center -8931 Colonial Center DriveFort Myers FL 33905
Department: Clinical Research RCC
Work Type: Full Time
Shift: Shift 1/8:00:00AM to 4:30:00PM
Minimum to Midpoint Pay Rate:$21.54 - $26.93 / hour
Summary
The primary responsibilities of a Clinical Research Coordinator (CRC) are; patent accrual, data management, protocol administration, and patient education. Patient accrual encompasses identifying eligible patients for LMHS IRC approved Clinical Trials. Data Management encompasses the on-study and long-term data management of every patient entered into a LMHS Clinical Trial. Protocol Administration encompasses maintaining protocol compliance with cooperative groups and adhering to the LMHS IRC guidelines. The last component is patient education. The CRC is responsible for educating the patient, staff and physicians on LMHS IRC approved Clinical Trials.
Requirements
Educational Requirements
Degree/Diploma ObtainedProgram of StudyRequired/
Preferredand/or
Bachelor'sPreferred
Additional Requirements
Experience Requirements
Minimum Years RequiredArea of ExperienceRequired/
Preferredand/or
1 YearClinical trials data managementRequired
State of Florida Licensure Requirements
LicensesRequired/
Preferredand/or
Certifications/Registration Requirements
Certificates/RegistrationsRequired/
Preferredand/or
Good communication skills, good computer skills, including word, Excel and navigating the Internet. Good customer service skills are required.
US:FL:Fort Myers
Department: Clinical Research RCC
Work Type: Full Time
Shift: Shift 1/8:00:00AM to 4:30:00PM
Minimum to Midpoint Pay Rate:$21.54 - $26.93 / hour
Summary
The primary responsibilities of a Clinical Research Coordinator (CRC) are; patent accrual, data management, protocol administration, and patient education. Patient accrual encompasses identifying eligible patients for LMHS IRC approved Clinical Trials. Data Management encompasses the on-study and long-term data management of every patient entered into a LMHS Clinical Trial. Protocol Administration encompasses maintaining protocol compliance with cooperative groups and adhering to the LMHS IRC guidelines. The last component is patient education. The CRC is responsible for educating the patient, staff and physicians on LMHS IRC approved Clinical Trials.
Requirements
Educational Requirements
Degree/Diploma ObtainedProgram of StudyRequired/
Preferredand/or
Bachelor'sPreferred
Additional Requirements
Experience Requirements
Minimum Years RequiredArea of ExperienceRequired/
Preferredand/or
1 YearClinical trials data managementRequired
State of Florida Licensure Requirements
LicensesRequired/
Preferredand/or
Certifications/Registration Requirements
Certificates/RegistrationsRequired/
Preferredand/or
Good communication skills, good computer skills, including word, Excel and navigating the Internet. Good customer service skills are required.
US:FL:Fort Myers
Additional Details
- City
- Fort Myers
- State
- Florida
- Country
- US
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