Clinical Research Nurse Jobs in Florida
Clinical Research Nurse jobs in Florida are consistently in demand, with strong activity concentrated in academic medical centers, oncology networks, and pharmaceutical trial sites serving one of the country's largest and fastest-growing patient populations, across experience levels from new graduate to senior research coordinator. The largest hiring activity is in Miami, Tampa, and Orlando, where institutions like Moffitt Cancer Center, Baptist Health South Florida, and AdventHealth maintain active clinical trial programs. Oncology, cardiology, and infectious disease trials are the most sought-after specialties for research nurses in Florida. Find a role that fits below and apply directly.
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Showing 5 of 154+ Clinical Research Nurse jobs
GENERAL SUMMARY
Clinical Research Coordinator works under Clinical Research Managers and are tasked with administering clinical trials. Responsibilities include managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.
Requirements:ESSENTIAL JOB FUNCTION/COMPETENCIES
The responsibilities and duties described in this job description are intended to provide a general overview of the position. Duties may vary depending on the specific needs of the affiliate or location you are working at and/or state requirements. Responsibilities include but are not limited to:
- Provide subject care and data collection procedures in adherence with the assigned study protocol and in accordance with good clinical research principals.
- Review subject charts, database records, and other sources to screen and identify potential subjects for inclusion in study based on criteria described in the protocol.
- Coordination and management of the clinical trial, communication with sponsor and authorities, visit coordination, sampling, time management and product accountability.
- Data collection and management, collection and development of source documents, use of CRFs, managing patient registration, AEs, filing and archiving, managing monitoring visits, dealing with queries.
- Maintain accurate records of the receipt, inventory, and dispensation of study drug and obtain and coordinate subject blood samples, cultures, tissues, and other specimens for laboratory analysis as described in study protocol.
- Patient visits, data collection and transcription/EDC, prepare for monitor visits, protocol adherence to include height, weight, blood pressure, respirations, pulse temperature, O2 saturation.
- Schedule appointments and organize materials to be used during study visits and ensure that all required tests are completed for each study visit per protocol.
- Includes initial study start-up information/ requirements, dissemination of updated Investigator’s Brochures, protocols and informed consent information, online training initiated by sponsor, review of correspondence throughout study.
- Completes Source Documentation-which includes completing and uploading all necessary documents to CRIO and maintaining all charts properly.
- Medical Assessment-includes obtaining information from patient or chart regarding name of medication, start and stop dates, dose, and indication.
- Biological Sampling Collection/Packaging/Shipping – includes serum and/or tissue collection, processing, packaging and shipping per study specific requirements.
- Case Report Form (CRF) Entries and Management – includes data entry, query resolution in paper and/or electronic CRFs.
- Investigational Product (IP) Management – includes receiving IP supplies, IP accountability, monitoring of temperature controls, destructions or return of IP.
- Develop and/or Maintain Essential Documents – includes study specific training documents, study specific logs, patient questionnaires, patient pill diaries, lab requisition forms, other study specific forms.
- Supply Chain Maintenance-Supplies Inventoried, stocking, organizing, and resupply order placed as required. Completed in Envi system.
- Study Coordination- rooming, administer questionnaires, scheduling scans, set up room for procedures and wipe and clean equipment after procedures and visits.
- Obtain/Maintain all required training- GCP, IATA,CPR Occasionally help the study coordinators at other offices such as the surgery center.
- Performs other position related duties as assigned.
- Employees shall adhere to high standards of ethical conduct and will comply with and assist in complying with all applicable laws and regulations. This will include and not be limited to following the Solaris Health Code of Conduct and all Solaris Health and Affiliated Practice policies and procedures; maintaining the confidentiality of patients' protected health information in compliance with the Health Insurance Portability and Accountability Act (HIPAA); immediately reporting any suspected concerns and/or violations to a supervisor and/or the Compliance Department; and the timely completion the Annual Compliance Training.
CERTIFICATIONS, LICENSURES OR REGISTRY REQUIREMENTS
- BLS certification required, ACLS preferred.
- License and certification as required by state.
KNOWLEDGE | SKILLS | ABILITIES
- Knowledge of medical terminology, healthcare coding systems, and clinics functions.
- Must be able to function in a team-oriented environment, display strong analytical, investigative, interpersonal and organizational skills, pay high attention to detail with consistent follow-through and be able to productively manage high volumes of work.
- Knowledge of database management.
- Maintain a working knowledge of all assigned study protocols and amendments.
- Excellent verbal and written communication skills.
- Skill in using computer programs and applications including Microsoft Office.
- Delivers exceptional patient service throughout all interactions.
- Excellent organizational skills and attention to detail.
- Strong analytical and problem-solving skills.
- Complies with all health and safety policies of the organization.
- Complies with HIPAA regulations for patient confidentiality.
- Ability to work independently and manage deadlines.
- Ability to establish and maintain effective working relationships with patients, colleagues, physicians and the public; successfully manages interactions with challenging or difficult people.
- Ability to deal compassionately, professionally, and courteously with patients, their families, physicians, and staff.
- Ability to build relationships with patients and display empathy and compassion to patients.
EDUCATION REQUIREMENTS
- High School Diploma or equivalent required.
- Bachelor’s degree in a related field (biology, psychology, nursing or healthcare) preferred.
EXPERIENCE REQUIREMENTS
- Experience with EPIC software preferred but not essential.
- 1-3 years of related experience preferred.
REQUIRED TRAVEL
- Minimal travel required.
PHYSICAL DEMANDS
Carrying Weight Frequency
1-25 lbs. Frequent from 34% to 66%
26-50 lbs. Occasionally from 2% to 33%
Pushing/Pulling Frequency
1-25 lbs. Seldom, up to 2%
100 + lbs. Seldom, up to 2%
Lifting - Height, Weight Frequency
Floor to Chest, 1 -25 lbs. Occasional: from 2% to 33%
Floor to Chest, 26-50 lbs. Seldom: up to 2%
Floor to Waist, 1-25 lbs. Occasional: from 2% to 33%
Floor to Waist, 26-50 lbs. Seldom: up to 2%
GENERAL SUMMARY
Clinical Research Coordinator works under Clinical Research Managers and are tasked with administering clinical trials. Responsibilities include managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.
Requirements:ESSENTIAL JOB FUNCTION/COMPETENCIES
The responsibilities and duties described in this job description are intended to provide a general overview of the position. Duties may vary depending on the specific needs of the affiliate or location you are working at and/or state requirements. Responsibilities include but are not limited to:
- Provide subject care and data collection procedures in adherence with the assigned study protocol and in accordance with good clinical research principals.
- Review subject charts, database records, and other sources to screen and identify potential subjects for inclusion in study based on criteria described in the protocol.
- Coordination and management of the clinical trial, communication with sponsor and authorities, visit coordination, sampling, time management and product accountability.
- Data collection and management, collection and development of source documents, use of CRFs, managing patient registration, AEs, filing and archiving, managing monitoring visits, dealing with queries.
- Maintain accurate records of the receipt, inventory, and dispensation of study drug and obtain and coordinate subject blood samples, cultures, tissues, and other specimens for laboratory analysis as described in study protocol.
- Patient visits, data collection and transcription/EDC, prepare for monitor visits, protocol adherence to include height, weight, blood pressure, respirations, pulse temperature, O2 saturation.
- Schedule appointments and organize materials to be used during study visits and ensure that all required tests are completed for each study visit per protocol.
- Includes initial study start-up information/ requirements, dissemination of updated Investigator’s Brochures, protocols and informed consent information, online training initiated by sponsor, review of correspondence throughout study.
- Completes Source Documentation-which includes completing and uploading all necessary documents to CRIO and maintaining all charts properly.
- Medical Assessment-includes obtaining information from patient or chart regarding name of medication, start and stop dates, dose, and indication.
- Biological Sampling Collection/Packaging/Shipping – includes serum and/or tissue collection, processing, packaging and shipping per study specific requirements.
- Case Report Form (CRF) Entries and Management – includes data entry, query resolution in paper and/or electronic CRFs.
- Investigational Product (IP) Management – includes receiving IP supplies, IP accountability, monitoring of temperature controls, destructions or return of IP.
- Develop and/or Maintain Essential Documents – includes study specific training documents, study specific logs, patient questionnaires, patient pill diaries, lab requisition forms, other study specific forms.
- Supply Chain Maintenance-Supplies Inventoried, stocking, organizing, and resupply order placed as required. Completed in Envi system.
- Study Coordination- rooming, administer questionnaires, scheduling scans, set up room for procedures and wipe and clean equipment after procedures and visits.
- Obtain/Maintain all required training- GCP, IATA,CPR Occasionally help the study coordinators at other offices such as the surgery center.
- Performs other position related duties as assigned.
- Employees shall adhere to high standards of ethical conduct and will comply with and assist in complying with all applicable laws and regulations. This will include and not be limited to following the Solaris Health Code of Conduct and all Solaris Health and Affiliated Practice policies and procedures; maintaining the confidentiality of patients' protected health information in compliance with the Health Insurance Portability and Accountability Act (HIPAA); immediately reporting any suspected concerns and/or violations to a supervisor and/or the Compliance Department; and the timely completion the Annual Compliance Training.
CERTIFICATIONS, LICENSURES OR REGISTRY REQUIREMENTS
- BLS certification required, ACLS preferred.
- License and certification as required by state.
KNOWLEDGE | SKILLS | ABILITIES
- Knowledge of medical terminology, healthcare coding systems, and clinics functions.
- Must be able to function in a team-oriented environment, display strong analytical, investigative, interpersonal and organizational skills, pay high attention to detail with consistent follow-through and be able to productively manage high volumes of work.
- Knowledge of database management.
- Maintain a working knowledge of all assigned study protocols and amendments.
- Excellent verbal and written communication skills.
- Skill in using computer programs and applications including Microsoft Office.
- Delivers exceptional patient service throughout all interactions.
- Excellent organizational skills and attention to detail.
- Strong analytical and problem-solving skills.
- Complies with all health and safety policies of the organization.
- Complies with HIPAA regulations for patient confidentiality.
- Ability to work independently and manage deadlines.
- Ability to establish and maintain effective working relationships with patients, colleagues, physicians and the public; successfully manages interactions with challenging or difficult people.
- Ability to deal compassionately, professionally, and courteously with patients, their families, physicians, and staff.
- Ability to build relationships with patients and display empathy and compassion to patients.
EDUCATION REQUIREMENTS
- High School Diploma or equivalent required.
- Bachelor’s degree in a related field (biology, psychology, nursing or healthcare) preferred.
EXPERIENCE REQUIREMENTS
- Experience with EPIC software preferred but not essential.
- 1-3 years of related experience preferred.
REQUIRED TRAVEL
- Minimal travel required.
PHYSICAL DEMANDS
Carrying Weight Frequency
1-25 lbs. Frequent from 34% to 66%
26-50 lbs. Occasionally from 2% to 33%
Pushing/Pulling Frequency
1-25 lbs. Seldom, up to 2%
100 + lbs. Seldom, up to 2%
Lifting - Height, Weight Frequency
Floor to Chest, 1 -25 lbs. Occasional: from 2% to 33%
Floor to Chest, 26-50 lbs. Seldom: up to 2%
Floor to Waist, 1-25 lbs. Occasional: from 2% to 33%
Floor to Waist, 26-50 lbs. Seldom: up to 2%
See All 154+ Clinical Research Nurse Jobs in Florida
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Find Clinical Research Nurse JobsClinical Research Nurse Jobs by City in Florida
Where Florida roles are concentrated, by current openings.
Clinical Research Nurse Job Market in Florida
A snapshot from current Florida openings, updated as new roles post.
Who's Hiring
- University of Miami19
- Moffitt Cancer Center13
- University of South Florida9
- University of Florida7
- Alcanza Clinical Research7
Top Industries Hiring
- Education15
- Healthcare & Medical Services10
- Biotechnology & Pharmaceuticals1
What Florida Employers Look For
The qualifications that appear most often in clinical research nurse jobs across Florida.
- Active Florida Registered Nurse license issued by the Florida Board of Nursing
- Minimum two years of clinical nursing experience in a hospital or specialty setting
- Familiarity with Good Clinical Practice guidelines and FDA-regulated trial protocols
- Experience with electronic data capture systems such as REDCap or Medidata Rave
- Current SOCRA or ACRP certification or demonstrated progress toward certification
- Strong ability to obtain informed consent and educate diverse patient populations
Clinical Research Nurse Jobs in Florida: Frequently Asked Questions
How do you become a clinical research nurse in Florida?
Start by obtaining an active Registered Nurse license through the Florida Board of Nursing, which requires passing the NCLEX-RN after completing an accredited nursing program. From there, most Florida employers expect at least one to two years of bedside clinical experience before transitioning into research. Pursuing a Good Clinical Practice certification through SOCRA or ACRP strengthens your application considerably, and many trial sites at Florida academic medical centers specifically look for that credential.
Which companies hire clinical research nurses in Florida?
Employers hiring clinical research nurses in Florida right now include University of Miami, Moffitt Cancer Center, and University of South Florida, based on current listings on Migrate Mate as of August 2026. Florida's dense concentration of NCI-designated cancer centers, large hospital systems, and contract research organizations operating out of Miami, Tampa, and Orlando means the hiring pool is broad and relatively consistent throughout the year.
Which Florida cities have the most clinical research nurse jobs?
Miami, Tampa, and Hollywood account for the most clinical research nurse openings in Florida. Miami drives volume through its international patient base and large academic research infrastructure, Tampa is anchored by Moffitt Cancer Center and University of South Florida Health, and Orlando's growth reflects AdventHealth's expanding trial portfolio alongside a rising number of contract research organizations choosing Central Florida for its logistics and population access.
Are there remote clinical research nurse jobs in Florida?
Yes, but they're rare. Most clinical research nurse work requires direct patient contact for screening, consent, specimen collection, and safety monitoring, making full remote work uncommon. About 16% of clinical research nurse openings tied to Florida are remote or hybrid as of August 2026, and those positions tend to involve data review, regulatory documentation, or study coordination duties that don't require on-site patient interaction.
How can I get hired as a clinical research nurse in Florida with little or no experience?
The most realistic entry path is applying to clinical research coordinator or research assistant roles at Florida hospital systems that allow nurses to transition from bedside units into research support positions. Moffitt Cancer Center and AdventHealth both run structured onboarding tracks for nurses new to research, and many oncology and infectious disease units at large Miami and Tampa hospitals hire research nurses from their own med-surg or ICU floors. Completing a Good Clinical Practice training course and volunteering on an Institutional Review Board committee adds visible credential weight for candidates without formal research experience.
Where can I find and apply to clinical research nurse jobs in Florida?
You can find and apply to clinical research nurse jobs in Florida on Migrate Mate, which lists current Florida openings updated regularly. Find roles that fit your experience and specialty interest, then apply directly to the employer. No signup is required to search and review what's currently available.
See All 154+ Clinical Research Nurse Jobs in Florida
Find roles in Florida that match your experience and apply in just a few clicks.
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