Research Jobs in Florida
Research jobs in Florida are concentrated in life sciences, clinical trials, marine and environmental science, and academic and defense-related fields, with openings at every level from research associate to principal investigator. Miami, Tampa, and Orlando anchor the bulk of the hiring, where institutions like the University of Florida Health, Moffitt Cancer Center, and Lockheed Martin maintain large and active research operations. The most in-demand specialties right now are clinical research coordination, biomedical research, and environmental and data-driven policy research. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 180+ Research jobs
Description
Job Summary
Under direction of a Research Clinical Trial Operations leader, the Lead Clinical Research Coordinator CTO will independently coordinate and will be accountable for the overall administration and outcome of multiple clinical studies within the Clinical Trials Office, requiring advanced-level knowledge and skills, involving human subjects that are being conducted within the Nicklaus Children's Research Institute. Ensures processes are in place and roles are defined in order for studies to be conducted smoothly and compliantly, avoiding delays or errors with patient registration/enrollment and/or documentation and in accordance with protocol requirements. Responsible for subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, report writing, and correspondence with investigators, IRBs, sponsors, CRO's and regulatory authorities. Provides guidance, training, and mentorship to Clinical Research Coordinators, Research Assistants and/or other support personnel.
Job Specific Duties
- Serves as a subject-matter expert and resource for the research team on the compliant conduct of assigned studies.
- Facilitates communication between investigators and Clinical Research Coordinators on subject-matter or technical matters.
- Oversees study conduct including all support data collection for study start-up activities.
- Oversees collection, maintenance, and reporting of accurate patient data for submissions to sponsors, maintaining patient records, and coordinating the collection and shipments of specimens as required by protocol.
- Reviews and confirms subject study eligibility with PI/Sub-I of assigned studies.
- Oversees study registration, patient screening/enrollment, and overall study requirements.
- Registers and enrolls research participants.
- Aggregates, tracks, trends, and reports research study and patient screening/enrollment data as required.
- Interacts with patients and families to recruit (screen, consent, and enroll) study subjects and ensures compliance with the protocol.
- Complies with the Research Finance Compliance policies and procedures including time and effort reporting for grants.
- Submits protocol amendments and other documents requiring IRB submission to the Research Regulatory Affairs team and notifies CTMS support staff for protocol digitization.
- Enters Research Patient information into CTMS within 72 hours of enrollment, patient visit, or patient-related event.
- Pre-screens potential research participants and enters information into CTMS within real time (if possible) or within 24 hours.
- Compiles accurate CTMS metrics data for updating SAC CTO slides and runs weekly enrollment reports for management review.
- Updates study statuses in CTMS and ensures study enrollment changes are communicated to Research Regulatory Affairs team and CTO Management.
- Attends meetings with Research management, research team, and/or PI/Sub-Is and is prepared to discuss research portfolio and/or patient status.
Qualifications
Minimum Job Requirements
- Bachelor's Degree Bachelor's degree or higher and 5 years of research experience (OR) 9 years of research experience. (Required)
- Clinical research certification through SOCRA or ACRP (CCRC, CCRP, CRA) required within 16 months in position
Knowledge, Skills, and Abilities
- Bachelor's degree in Nursing (BSN) and/or current RN licensure strongly preferred.
- Ability to train, guide, and mentor peers.
- Knowledge of rules and regulations governing the designated research.
- Ability to use logical and scientific thinking to interpret technical data and solve a broad range of problems.
- Bilingual in English/Spanish.
- Excellent communication skills in working with both children and adults.
- Software applications experience including word processing, scheduling and contact database, email, web browsing, hospital records, other database software and office equipment.
- Experience with relevant hospital equipment for each clinical trial project.
- Experience working on clinical trials, interventional studies all phases.
- Advanced knowledge of investigational protocols (data management, query resolution, protocol design and protocol implementation).
- Demonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital.
- Excellent ability to organize/prioritize workload effectively to meet deadlines in an environment with multiple interruptions and changing priorities. Meticulous attention to detail.
- Ability to respond calmly under stressful conditions.
- Ability to maintain confidentiality of sensitive information.
- Ability to effectively work in a team.
- Excellent time management and interpersonal skills.
Job:
ResearchJob:
Department:
RI - ADMINISTRATION-2100-380950
Job Status:
ProfessionalDescription
Job Summary
Under direction of a Research Clinical Trial Operations leader, the Lead Clinical Research Coordinator CTO will independently coordinate and will be accountable for the overall administration and outcome of multiple clinical studies within the Clinical Trials Office, requiring advanced-level knowledge and skills, involving human subjects that are being conducted within the Nicklaus Children's Research Institute. Ensures processes are in place and roles are defined in order for studies to be conducted smoothly and compliantly, avoiding delays or errors with patient registration/enrollment and/or documentation and in accordance with protocol requirements. Responsible for subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, report writing, and correspondence with investigators, IRBs, sponsors, CRO's and regulatory authorities. Provides guidance, training, and mentorship to Clinical Research Coordinators, Research Assistants and/or other support personnel.
Job Specific Duties
- Serves as a subject-matter expert and resource for the research team on the compliant conduct of assigned studies.
- Facilitates communication between investigators and Clinical Research Coordinators on subject-matter or technical matters.
- Oversees study conduct including all support data collection for study start-up activities.
- Oversees collection, maintenance, and reporting of accurate patient data for submissions to sponsors, maintaining patient records, and coordinating the collection and shipments of specimens as required by protocol.
- Reviews and confirms subject study eligibility with PI/Sub-I of assigned studies.
- Oversees study registration, patient screening/enrollment, and overall study requirements.
- Registers and enrolls research participants.
- Aggregates, tracks, trends, and reports research study and patient screening/enrollment data as required.
- Interacts with patients and families to recruit (screen, consent, and enroll) study subjects and ensures compliance with the protocol.
- Complies with the Research Finance Compliance policies and procedures including time and effort reporting for grants.
- Submits protocol amendments and other documents requiring IRB submission to the Research Regulatory Affairs team and notifies CTMS support staff for protocol digitization.
- Enters Research Patient information into CTMS within 72 hours of enrollment, patient visit, or patient-related event.
- Pre-screens potential research participants and enters information into CTMS within real time (if possible) or within 24 hours.
- Compiles accurate CTMS metrics data for updating SAC CTO slides and runs weekly enrollment reports for management review.
- Updates study statuses in CTMS and ensures study enrollment changes are communicated to Research Regulatory Affairs team and CTO Management.
- Attends meetings with Research management, research team, and/or PI/Sub-Is and is prepared to discuss research portfolio and/or patient status.
Qualifications
Minimum Job Requirements
- Bachelor's Degree Bachelor's degree or higher and 5 years of research experience (OR) 9 years of research experience. (Required)
- Clinical research certification through SOCRA or ACRP (CCRC, CCRP, CRA) required within 16 months in position
Knowledge, Skills, and Abilities
- Bachelor's degree in Nursing (BSN) and/or current RN licensure strongly preferred.
- Ability to train, guide, and mentor peers.
- Knowledge of rules and regulations governing the designated research.
- Ability to use logical and scientific thinking to interpret technical data and solve a broad range of problems.
- Bilingual in English/Spanish.
- Excellent communication skills in working with both children and adults.
- Software applications experience including word processing, scheduling and contact database, email, web browsing, hospital records, other database software and office equipment.
- Experience with relevant hospital equipment for each clinical trial project.
- Experience working on clinical trials, interventional studies all phases.
- Advanced knowledge of investigational protocols (data management, query resolution, protocol design and protocol implementation).
- Demonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital.
- Excellent ability to organize/prioritize workload effectively to meet deadlines in an environment with multiple interruptions and changing priorities. Meticulous attention to detail.
- Ability to respond calmly under stressful conditions.
- Ability to maintain confidentiality of sensitive information.
- Ability to effectively work in a team.
- Excellent time management and interpersonal skills.
Job:
ResearchJob:
Department:
RI - ADMINISTRATION-2100-380950
Job Status:
ProfessionalSee All 180+ Research Jobs in Florida
Find roles in Florida that match your experience and apply in just a few clicks.
Find Research JobsResearch Jobs by City in Florida
Where Florida roles are concentrated, by current openings.
Research Job Market in Florida
A snapshot from current Florida openings, updated as new roles post.
Who's Hiring
- University of Miami24
- University of Florida15
- University of South Florida15
- Moffitt Cancer Center14
- Fortrea5
Top Industries Hiring
- Education13
- Healthcare & Medical Services8
- Biotechnology & Pharmaceuticals2
What Florida Employers Look For
The qualifications that appear most often in research jobs across Florida.
- Bachelor's or advanced degree in a relevant scientific, social science, or technical field
- Demonstrated experience designing studies, collecting data, and analyzing results
- Proficiency with statistical software such as SAS, SPSS, R, or Python
- Familiarity with IRB protocols, GCP guidelines, or federal research compliance standards
- Strong written communication skills for grant writing, reports, and peer collaboration
- Experience with literature reviews, data management systems, or laboratory techniques
Research Jobs in Florida: Frequently Asked Questions
How do you become a research in Florida?
Most research roles in Florida require at minimum a bachelor's degree in a field relevant to the position, such as biology, public health, psychology, or engineering, with many positions at universities and hospitals preferring a master's or doctorate. Florida does not issue a single statewide research license, but clinical research coordinators working on human subjects studies typically complete the Collaborative Institutional Training Initiative certification, which most Florida academic medical centers and trial sponsors require before study participation.
Which companies hire researchs in Florida?
Employers hiring researchs in Florida right now include University of Miami, University of Florida, and University of South Florida, based on current listings on Migrate Mate as of August 2026. Florida's deep concentration of academic medical centers, defense contractors, and marine science institutions means research hiring is spread across both the private sector and large public universities throughout the state.
Which Florida cities have the most research jobs?
Tampa, Miami, and Gainesville account for the largest share of research openings in Florida. Miami draws heavily from clinical and public health research tied to its major hospital networks, Tampa is anchored by Moffitt Cancer Center and the University of South Florida's research enterprise, and Orlando's growth reflects both the University of Central Florida and expanding biotech and defense research corridors in the region.
Are there remote research jobs in Florida?
Yes, but they're less common than in purely desk-based fields, since many research roles require lab access, clinical site presence, or direct data collection. About 33% of research openings tied to Florida are remote or hybrid as of August 2026, which reflects the mixed nature of the field. The positions most likely to be fully remote are those focused on data analysis, literature synthesis, grant writing, or survey-based social science research.
How can I get hired as a research in Florida with little or no experience?
The most realistic entry point for candidates without formal research experience in Florida is a research assistant or research coordinator I position at a university health system or academic institution. Moffitt Cancer Center, UF Health, and AdventHealth all run structured programs for early-career candidates, and Florida's public universities frequently post paid research assistant roles open to recent graduates. Completing the Collaborative Institutional Training Initiative certification before applying and targeting postings that list it as preferred rather than required gives candidates without prior experience a meaningful edge.
Where can I find and apply to research jobs in Florida?
You can find and apply to research jobs in Florida on Migrate Mate, which lists current openings across the state. Search for roles that match your specialty and experience level, then apply directly to the ones that fit your background.
See All 180+ Research Jobs in Florida
Find roles in Florida that match your experience and apply in just a few clicks.
Find Research Jobs