Clinical Research Jobs in Florida
Clinical Research jobs in Florida are in strong demand, concentrated in pharmaceutical and biotech companies, academic medical centers, and contract research organizations, with openings at every level from research assistant and coordinator through principal investigator and director. Miami, Tampa, and Orlando are the primary hiring hubs, anchored by established employers such as Johnson & Johnson, Pfizer, and the University of Miami Health System. Clinical data management, oncology trials, and regulatory affairs are among the most consistently sought specialties in the state. Find a role that fits below and apply directly.
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Showing 5 of 154+ Clinical Research 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 Jobs in Florida
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Find Clinical Research JobsClinical Research Jobs by City in Florida
Where Florida roles are concentrated, by current openings.
Clinical Research 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 jobs across Florida.
- Bachelor's degree in life sciences, nursing, or a related clinical field
- ACRP or SOCRA clinical research certification preferred or required
- Experience with FDA regulations, ICH-GCP guidelines, and IRB submission processes
- Proficiency in electronic data capture systems such as Medidata Rave or Oracle InForm
- Strong knowledge of clinical trial protocols, informed consent, and adverse event reporting
- Excellent attention to detail and ability to manage multiple active study sites simultaneously
Clinical Research Jobs in Florida: Frequently Asked Questions
How do you become a clinical research professional in Florida?
Most clinical research roles in Florida require at least a bachelor's degree in a life science, nursing, or health-related field, followed by entry-level work as a research assistant or coordinator. Florida has no state-specific clinical research license, but employers broadly expect candidates to hold or pursue certification from the Association of Clinical Research Professionals or the Society of Clinical Research Associates. Many roles at Florida academic medical centers also require completion of Good Clinical Practice training before starting.
Which companies hire clinical research professionals in Florida?
Employers hiring clinical research professionals 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 large concentration of contract research organizations, pharmaceutical manufacturers, and academic health systems keeps hiring active across the state year-round.
Which Florida cities have the most clinical research jobs?
Miami, Tampa, and Hollywood are the Florida cities with the most clinical research openings, reflecting the concentration of academic medical centers, large hospital networks, and pharmaceutical and biotech companies in those metro areas, while smaller markets like Gainesville and Jacksonville contribute additional volume through their own university health systems and research institutes.
Are there remote clinical research jobs in Florida?
Yes, but they're limited. Clinical research work is largely site-based, requiring direct patient contact, on-site monitoring, and hands-on trial management that cannot be done remotely. About 16% of clinical research openings tied to Florida are remote or hybrid as of August 2026, and those positions tend to be in data management, regulatory affairs, or sponsor-side clinical monitoring roles rather than coordinator or site-based positions.
How can I get hired as a clinical research professional in Florida with little or no experience?
The most realistic entry path is an entry-level research coordinator or research assistant role at a Florida academic medical center or hospital, where institutions such as the University of Florida Health, Moffitt Cancer Center, and AdventHealth regularly hire candidates without prior trial experience. A completed Good Clinical Practice certification, a background in healthcare administration, nursing, or laboratory work, and any volunteer or intern experience with an Institutional Review Board submission gives candidates a clear edge with these employers.
Where can I find and apply to clinical research jobs in Florida?
You can find and apply to clinical research jobs in Florida on Migrate Mate, which lists current Florida openings across all experience levels, specialties, and major hiring markets. Find roles that fit your background and apply directly.
See All 154+ Clinical Research Jobs in Florida
Find roles in Florida that match your experience and apply in just a few clicks.
Find Clinical Research Jobs