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BayCare·St Josephs · Tampa, FL

Clinical Research Coordinator

Healthcare AdministrationFull timeDays
iPosting details
ScheduleDays · Full time
RequirementsRRT · LPN license
EducationBachelor's degree · Associate degree
Experience2+ years
SourceBayCare · posted Sep 23, 2026
✓Requirements
Licensure
✓Or - 5 years LPN experience and 1 year coordinator role with a Technical School and LPN License
✓Or - 2 years LPN and 5 years Research with a Technical School and LPN License
✓Or - 7 years research experience with a Technical School and LPN License
✓Perform duties as assigned under the scope of related certification or licensure
Certifications
✓The required education/experience/certification for each level is outlined below
✓RRT certification
Education
✓Required - Bachelor's degree in related field in lieu of experience
✓Or - 5 years of research experience with a High School Diploma and CCRP (Clinical Research) or CCRC (Clinical Research)
✓Or - 2 years research experience with a Bachelor's degree in a related field
✓Associate degree
Qualifications
✓Ensure study start-up completion worksheet is complete with required protocol specific training of research staff and ancillary departments
+Benefits
✓Medical, dental and vision
✓401(k) with match
✓Paid time off
✓Tuition assistance
+St Josephs
1,354beds
4administration roles open
TampaFL
Pay for this position
Pay not listed
Apply to BayCareContact Recruiter about this role
✓You’ll need
Licensure
✓Or - 5 years LPN experience and 1 year coordinator role with a Technical School and LPN License
✓Or - 2 years LPN and 5 years Research with a Technical School and LPN License
✓Or - 7 years research experience with a Technical School and LPN License
✓Perform duties as assigned under the scope of related certification or licensure
Certifications
✓The required education/experience/certification for each level is outlined below
✓RRT certification
Education
✓Required - Bachelor's degree in related field in lieu of experience
✓Or - 5 years of research experience with a High School Diploma and CCRP (Clinical Research) or CCRC (Clinical Research)
✓Or - 2 years research experience with a Bachelor's degree in a related field
✓Associate degree
Qualifications
✓Ensure study start-up completion worksheet is complete with required protocol specific training of research staff and ancillary departments
+Benefits
Medical, dental and vision401(k) with matchPaid time offTuition assistance

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About the role

Ensure study start-up completion worksheet is complete with required protocol specific training of research staff and ancillary departments

What you’ll do
Facilitate protocol development, CompleteFacilitate protocol development, Complete trial feasibility
Ensure study start-up completionEnsure study start-up completion worksheet is complete with required protocol specific training of research staff and ancillary departments
Ensure adherence to theEnsure adherence to the study protocol and schedule of events, patient visit scheduling for protocol related procedures
Preparation of IRB reportsPreparation of IRB reports
Establishment and maintenance ofEstablishment and maintenance of regulatory documents