Research Jobs in Miami, FL
Research jobs in Miami are concentrated in biomedical sciences, academic institutions, and healthcare systems across Brickell, the Health District, and Coral Gables, with strong demand from life sciences companies, university research centers, and hospital networks. Employers hiring right now include University of Miami, Florida International University, and Evolution Research. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 167+ Research jobs
Current Employees:
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this tip sheet.
The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Clinical Research Nurse 2 to work at the UHealth campus in Miami, Fl.
CORE JOB SUMMARY
The Clinical Research Nurse 2 ensures the integrity and quality of clinical research studies are maintained and conducted in accordance with practice guidelines, federal and sponsor regulations, and institutional policies and procedures. Additionally, the Clinical Research Nurse 2 plays a key role in the recruitment of participants and achievement of research objectives.
CORE JOB FUNCTIONS
- Assesses, troubleshoots, and reports problems with data collection to appropriate managing staff.
- Identifies desired research outcomes and evaluates and monitors subjects’ responses.
- Conducts initiation visits and registers patients in clinical studies.
- Performs study data collection and entry using charts, correspondence, medical records, and relevant communications. Identifies and procures equipment and supplies needed to fulfill project requirements.
- Educates staff and subjects about protocols, treatment, possible side effects, and complications. May also collect and handle specimens as required by individual study protocols.
- Prepares and processes new research proposals and amendments and continually monitors applications and adverse events.
- Assists with study completion, data lock, study closeout, and archiving of study files to ensure completeness and continuity of all study data.
- Completes ongoing checks of clinical data entered on the case report forms to ensure accuracy and revises any discrepancies.
- Adheres to University and unit-level policies and procedures and safeguards University assets.
CORE QUALIFICATIONS
Education: Bachelor’s degree in relevant field required.
Certification and Licensing: Valid State of Florida RN license required, and the BLS certification.
Experience: Minimum 3 years of relevant experience required.
Knowledge, Skills and Abilities:
- Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands.
- Teamwork: Ability to work collaboratively with others and contribute to a team environment.
- Technical Proficiency: Skilled in using office software, technology, and relevant computer applications.
- Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders.
DEPARTMENT SPECIFICS
The Clinical Research Nurse 2 delivers patient-family centered care in a culturally competent manner utilizing evidence-based standards of quality, safety, and service while ensuring population-specific patient care and compliance with the research protocol in an ambulatory setting. The Clinical Research Nurse 2 plays a key role in the recruitment of participants and achievement of research objectives. Additionally, ensures that the integrity and quality of clinical research studies is maintained and that studies are conducted in accordance with practice guidelines, federal and sponsor regulations, and institutional policies and procedures. Provides care to patients, practicing in accordance with the Scope and Standards of Nursing Practice of the Florida Nursing Practice Act, regulatory requirements, standards of care and institutional policies and procedures. Within that role, the Clinical Research Nurse 2 performs all steps of the nursing process including assessing/screening of patients; interpreting data; planning, implementing, and evaluating care; coordinating care with other providers; and teaching the patient and family the knowledge and skills needed to manage their care and prevent complications while ensuring compliance with the research protocol. As a professional, monitors the quality of nursing care provided and nurtures a compassionate environment. The Clinical Research Nurse 2 delivers care that supports the UHealth mission to be a state-of-the-art academic medical center by participating in transforming patient care through innovative research.
CORE QUALIFICATIONS
Education: Bachelor of Science in nursing required.
Certification and Licensing: Current Florida Registered Nurse license; Current American Heart Association (AHA) Basic Life Support (BLS) for healthcare providers Certification Oncology Nursing Society (ONS) provider card for Chemotherapy and Immunotherapy administration.
Certification in relevant specialty or field (i.e., oncology, clinical research, etc.) preferred.
Experience: Minimum of 3 years of relevant experience.
Knowledge, Skills and Attitudes:
- Strong, effective communication skills with patients, families, and clinical team for innovative patient care and trust.
- Ability to collaborate with peers in the best interest of the patient to provide consistent quality of care.
- Ability to establish and maintain positive, caring relationships with executives, managers, physicians, non-physician providers, patients/families and other departments and staff.
- Ability to adapt and exhibit flexibility to handle new, different, or changing environments.
- Demonstrates strong time management skills to prioritize, triage, and act proactively.
- Ability to uphold professional ethics and maintain patient confidentiality.
- Knowledgeable on all aspects of patient care including assessing, planning, coordinating, monitoring, and evaluating the patients’ progress through continuum of care.
- Knowledge in navigating the electronic medical records and reviewing treatment plans.
- Skill in completing assignments accurately and with attention to detail.
- Ability to work evenings, nights, and weekends as necessary.
- Commitment to the University’s core values.
- Ability to work independently and/or in a collaborative environment.
- Critical thinking, analytical and problem-solving abilities required as related to various aspects of the protocol.
- Good reading, writing, mathematical, organizational and comprehension skills.
- Demonstrate ability to maintain cooperative working relationships with internal and external units in a clinical research environment.
Department Specific Functions
-
Incorporates the University mission, vision, values, and code of Business Conduct into planning research related patient care and clinical trials activities.
-
Completes all University and department specific required trainings prior to beginning research related activities.
-
Provides clinical trial support in the hospital and/or clinic setting to ensure University patients are offered appropriate clinical trials following Good Clinical Practice standards.
-
Screens patients/patient records to identify potential trial candidates and notify the treating physician and University Clinical Research Staff.
-
Assists the Investigator obtain subject informed consent following the University Clinical Research Staff Informed Consent Process 301-05. This involves spending time with the patient and family to provide detailed information about the clinical trial and answer any questions arising within the Clinical Research Nurse scope of knowledge.
-
Educates staff and subjects about protocols, treatment, possible side effects, and complications.
-
Maintains expert knowledge of adverse events and policies regarding reporting.
-
With input as required from the Investigator, assesses and documents adverse events and concomitant medications.
-
Works closely with the protocol University Clinical Research Staff to ensure Serious Adverse Events are documented and reported per protocol and regulatory requirements.
-
Assesses and documents the patient’s compliance and response to protocol treatment.
-
Prepares and reviews necessary data for monitoring visits, audits, and safety summaries.
-
Demonstrate the ability to support a clinical audit, including preparation, participation, documentation and follow up.
-
Collaborates closely with protocol University Clinical Research Staff. Provides University Clinical Research Staff with the Informed Consent Document Form and all source documentation required to determine eligibility and maintain compliance.
-
Works closely with the Investigator, Investigational Pharmacist, Comprehensive Treatment Unit (CTU) staff and Clinical Research Services Senior Manager to review the clinical trial treatment order-set and individual patient orders.
-
Provides potential and registered clinical trial patients with contact information to ensure that patients and families have an avenue to direct questions about the clinical trial that they were offered.
-
Enters applicable research related orders and research specific tests and procedures into the chart for the Investigator to sign.
-
Performs research related protocol specific ECGs.
-
Performs simple clinical tasks (research blood draws, vital signs etc.) according to scope of practice, skills, and competencies.
-
Provides conduit between physicians, allied health professionals, nursing staff and clinical trial patients regarding trial related issues to maintain a safe environment for the patient while maintaining compliance.
-
Ensures the effectiveness of protocol related education for patient and multidisciplinary team members.
-
Communicates with the Investigator, patients, families, clinical staff, and University Clinical Research Staff to ensure that treatment plans and research related interventions and activities are understood and scheduled appropriately.
-
Provides a consistent and accessible resource for physicians and clinical staff regarding clinical trials.
-
Works with the Investigator to ensure all clinical trial procedures are performed according to the protocol.
-
Receives clinical trial oral medication from pharmacy and administers the drug, documenting appropriately and providing source documents to the protocol University Clinical Research Staff.
-
Performs second chemotherapy order check prior to administration by another clinical trials nurse.
-
Demonstrates an understanding of and a commitment to customer service values of respect, courtesy, ownership, privacy, professionalism, and responsiveness. Initiates and maintains open communication with other members of the team to assure that the patient and family receive the full scope of interdisciplinary expertise and services along with care provided by participation in a clinical trial.
-
Completes mandatory education and training that includes review of age-specific needs and other competencies required by the University.
-
Attends Investigator meetings as required.
-
Maintains a safe working environment through compliance with established policies and procedures and timely reporting of safety variances.
-
Participates in the development of general goals of University Clinical Research Staff.
-
Adhere to all University policies and procedures.
-
Demonstrate the ability to implement a Corrective Action and Prevention Action (CAPA) assessment and follow CAPA related issues through to resolution.
-
Participates in professional activities beyond the departmental level.
-
Mentor and encourage clinical research staff to develop through participation in professional organizations, serving on committees, attending journal presentations, seminars, or conferences.
The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.
UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the groundbreaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.
The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.
Job Status:
Full time
Employee Type:
Staff
Current Employees:
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this tip sheet.
The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Clinical Research Nurse 2 to work at the UHealth campus in Miami, Fl.
CORE JOB SUMMARY
The Clinical Research Nurse 2 ensures the integrity and quality of clinical research studies are maintained and conducted in accordance with practice guidelines, federal and sponsor regulations, and institutional policies and procedures. Additionally, the Clinical Research Nurse 2 plays a key role in the recruitment of participants and achievement of research objectives.
CORE JOB FUNCTIONS
- Assesses, troubleshoots, and reports problems with data collection to appropriate managing staff.
- Identifies desired research outcomes and evaluates and monitors subjects’ responses.
- Conducts initiation visits and registers patients in clinical studies.
- Performs study data collection and entry using charts, correspondence, medical records, and relevant communications. Identifies and procures equipment and supplies needed to fulfill project requirements.
- Educates staff and subjects about protocols, treatment, possible side effects, and complications. May also collect and handle specimens as required by individual study protocols.
- Prepares and processes new research proposals and amendments and continually monitors applications and adverse events.
- Assists with study completion, data lock, study closeout, and archiving of study files to ensure completeness and continuity of all study data.
- Completes ongoing checks of clinical data entered on the case report forms to ensure accuracy and revises any discrepancies.
- Adheres to University and unit-level policies and procedures and safeguards University assets.
CORE QUALIFICATIONS
Education: Bachelor’s degree in relevant field required.
Certification and Licensing: Valid State of Florida RN license required, and the BLS certification.
Experience: Minimum 3 years of relevant experience required.
Knowledge, Skills and Abilities:
- Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands.
- Teamwork: Ability to work collaboratively with others and contribute to a team environment.
- Technical Proficiency: Skilled in using office software, technology, and relevant computer applications.
- Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders.
DEPARTMENT SPECIFICS
The Clinical Research Nurse 2 delivers patient-family centered care in a culturally competent manner utilizing evidence-based standards of quality, safety, and service while ensuring population-specific patient care and compliance with the research protocol in an ambulatory setting. The Clinical Research Nurse 2 plays a key role in the recruitment of participants and achievement of research objectives. Additionally, ensures that the integrity and quality of clinical research studies is maintained and that studies are conducted in accordance with practice guidelines, federal and sponsor regulations, and institutional policies and procedures. Provides care to patients, practicing in accordance with the Scope and Standards of Nursing Practice of the Florida Nursing Practice Act, regulatory requirements, standards of care and institutional policies and procedures. Within that role, the Clinical Research Nurse 2 performs all steps of the nursing process including assessing/screening of patients; interpreting data; planning, implementing, and evaluating care; coordinating care with other providers; and teaching the patient and family the knowledge and skills needed to manage their care and prevent complications while ensuring compliance with the research protocol. As a professional, monitors the quality of nursing care provided and nurtures a compassionate environment. The Clinical Research Nurse 2 delivers care that supports the UHealth mission to be a state-of-the-art academic medical center by participating in transforming patient care through innovative research.
CORE QUALIFICATIONS
Education: Bachelor of Science in nursing required.
Certification and Licensing: Current Florida Registered Nurse license; Current American Heart Association (AHA) Basic Life Support (BLS) for healthcare providers Certification Oncology Nursing Society (ONS) provider card for Chemotherapy and Immunotherapy administration.
Certification in relevant specialty or field (i.e., oncology, clinical research, etc.) preferred.
Experience: Minimum of 3 years of relevant experience.
Knowledge, Skills and Attitudes:
- Strong, effective communication skills with patients, families, and clinical team for innovative patient care and trust.
- Ability to collaborate with peers in the best interest of the patient to provide consistent quality of care.
- Ability to establish and maintain positive, caring relationships with executives, managers, physicians, non-physician providers, patients/families and other departments and staff.
- Ability to adapt and exhibit flexibility to handle new, different, or changing environments.
- Demonstrates strong time management skills to prioritize, triage, and act proactively.
- Ability to uphold professional ethics and maintain patient confidentiality.
- Knowledgeable on all aspects of patient care including assessing, planning, coordinating, monitoring, and evaluating the patients’ progress through continuum of care.
- Knowledge in navigating the electronic medical records and reviewing treatment plans.
- Skill in completing assignments accurately and with attention to detail.
- Ability to work evenings, nights, and weekends as necessary.
- Commitment to the University’s core values.
- Ability to work independently and/or in a collaborative environment.
- Critical thinking, analytical and problem-solving abilities required as related to various aspects of the protocol.
- Good reading, writing, mathematical, organizational and comprehension skills.
- Demonstrate ability to maintain cooperative working relationships with internal and external units in a clinical research environment.
Department Specific Functions
-
Incorporates the University mission, vision, values, and code of Business Conduct into planning research related patient care and clinical trials activities.
-
Completes all University and department specific required trainings prior to beginning research related activities.
-
Provides clinical trial support in the hospital and/or clinic setting to ensure University patients are offered appropriate clinical trials following Good Clinical Practice standards.
-
Screens patients/patient records to identify potential trial candidates and notify the treating physician and University Clinical Research Staff.
-
Assists the Investigator obtain subject informed consent following the University Clinical Research Staff Informed Consent Process 301-05. This involves spending time with the patient and family to provide detailed information about the clinical trial and answer any questions arising within the Clinical Research Nurse scope of knowledge.
-
Educates staff and subjects about protocols, treatment, possible side effects, and complications.
-
Maintains expert knowledge of adverse events and policies regarding reporting.
-
With input as required from the Investigator, assesses and documents adverse events and concomitant medications.
-
Works closely with the protocol University Clinical Research Staff to ensure Serious Adverse Events are documented and reported per protocol and regulatory requirements.
-
Assesses and documents the patient’s compliance and response to protocol treatment.
-
Prepares and reviews necessary data for monitoring visits, audits, and safety summaries.
-
Demonstrate the ability to support a clinical audit, including preparation, participation, documentation and follow up.
-
Collaborates closely with protocol University Clinical Research Staff. Provides University Clinical Research Staff with the Informed Consent Document Form and all source documentation required to determine eligibility and maintain compliance.
-
Works closely with the Investigator, Investigational Pharmacist, Comprehensive Treatment Unit (CTU) staff and Clinical Research Services Senior Manager to review the clinical trial treatment order-set and individual patient orders.
-
Provides potential and registered clinical trial patients with contact information to ensure that patients and families have an avenue to direct questions about the clinical trial that they were offered.
-
Enters applicable research related orders and research specific tests and procedures into the chart for the Investigator to sign.
-
Performs research related protocol specific ECGs.
-
Performs simple clinical tasks (research blood draws, vital signs etc.) according to scope of practice, skills, and competencies.
-
Provides conduit between physicians, allied health professionals, nursing staff and clinical trial patients regarding trial related issues to maintain a safe environment for the patient while maintaining compliance.
-
Ensures the effectiveness of protocol related education for patient and multidisciplinary team members.
-
Communicates with the Investigator, patients, families, clinical staff, and University Clinical Research Staff to ensure that treatment plans and research related interventions and activities are understood and scheduled appropriately.
-
Provides a consistent and accessible resource for physicians and clinical staff regarding clinical trials.
-
Works with the Investigator to ensure all clinical trial procedures are performed according to the protocol.
-
Receives clinical trial oral medication from pharmacy and administers the drug, documenting appropriately and providing source documents to the protocol University Clinical Research Staff.
-
Performs second chemotherapy order check prior to administration by another clinical trials nurse.
-
Demonstrates an understanding of and a commitment to customer service values of respect, courtesy, ownership, privacy, professionalism, and responsiveness. Initiates and maintains open communication with other members of the team to assure that the patient and family receive the full scope of interdisciplinary expertise and services along with care provided by participation in a clinical trial.
-
Completes mandatory education and training that includes review of age-specific needs and other competencies required by the University.
-
Attends Investigator meetings as required.
-
Maintains a safe working environment through compliance with established policies and procedures and timely reporting of safety variances.
-
Participates in the development of general goals of University Clinical Research Staff.
-
Adhere to all University policies and procedures.
-
Demonstrate the ability to implement a Corrective Action and Prevention Action (CAPA) assessment and follow CAPA related issues through to resolution.
-
Participates in professional activities beyond the departmental level.
-
Mentor and encourage clinical research staff to develop through participation in professional organizations, serving on committees, attending journal presentations, seminars, or conferences.
The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.
UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the groundbreaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.
The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.
Job Status:
Full time
Employee Type:
Staff
See All 167+ Research Jobs in Miami
Find roles in Miami that match your experience and apply in just a few clicks.
Find Research JobsResearch Job Market in Miami
Who's Hiring
- University of Miami90
- Florida International University18
- Evolution Research10
- Nicklaus Children's Health System10
- Baptist Health South Florida9
Top Industries Hiring
- Education80
- Healthcare & Medical Services20
- Science & Research6
- Insurance1
- Medical Devices1
Research Jobs in Miami: Frequently Asked Questions
How do I get a research job in Miami?
Focus on Miami's strongest research sectors: biomedical and clinical research centered in the Health District, marine and environmental science along the coast, and behavioral and social science through the city's universities. Candidates who can demonstrate lab technique, IRB protocol experience, or data management skills stand out. Connecting with research hospitals, university departments in Coral Gables, and biotech firms in Doral gives you the best local foothold.
Which companies hire researchs in Miami?
Miami research roles are posted by University of Miami, Florida International University, and Evolution Research and others right now, based on current listings on Migrate Mate as of July 2026. Miami's research employer base is anchored by academic medical centers, life sciences firms, and public health organizations, many clustered in the Health District and around the University of Miami's main campus.
Are there remote research jobs in Miami?
Yes, though it depends on the type of research work: desk-based and analytical roles such as literature review, data analysis, and regulatory writing are frequently remote, while lab-based and clinical positions require on-site presence. About 10% of research openings tied to Miami are remote or hybrid as of July 2026. Policy research, public health analysis, and survey-based social science roles tend to offer the most remote flexibility in Miami.
How can I get a research job in Miami with little or no experience?
The most realistic entry path in Miami is a research assistant or study coordinator role at one of the city's hospital networks or university-affiliated research centers. Jackson Health System, the University of Miami Miller School of Medicine, and Florida International University regularly bring on entry-level staff to support ongoing studies. Familiarity with REDCap, basic data entry, and CITI certification are practical differentiators that open doors locally without requiring prior professional research experience.
Which industries hire the most researchs in Miami?
Most research openings in Miami sit in Education, Healthcare & Medical Services, and Science & Research, per current listings on Migrate Mate as of July 2026. Miami's concentration of teaching hospitals, international health organizations, and university-linked biotech initiatives makes healthcare and life sciences the dominant drivers of local research hiring, with public policy and environmental science rounding out demand.
See All 167+ Research Jobs in Miami
Find roles in Miami that match your experience and apply in just a few clicks.
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