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Patient Reported Outcomes Jobs in Florida (NOW HIRING)

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Surgical Care Navigator

Miami Beach, FL · On-site +1

$20.75 - $26.75/hr

Track and document patient-reported outcomes (PROs) and feedback. Clinical Collaboration * Serve as a liaison among patients, providers, and internal teams. * Promote evidence-based orthopedic care ...

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Patient Reported Outcomes information

What is a patient reported outcome?

Patient Reported Outcomes (PROs) are health data provided directly by patients, reflecting their own perspectives on their health condition, treatment, symptoms, and quality of life, without interpretation by healthcare providers. These outcomes are commonly collected using standardized questionnaires or surveys. PROs are vital in clinical trials and healthcare practices as they help assess the effectiveness of treatments from the patient's viewpoint, guiding both clinical decision-making and regulatory approvals.

How does a patient reported outcomes professional typically collaborate with clinical and research teams?

Professionals in Patient Reported Outcomes (PRO) regularly work alongside clinical researchers, statisticians, and regulatory teams to design, implement, and analyze patient-centered data collection tools. They often facilitate the integration of PRO measures into clinical trials, ensuring that patient perspectives on symptoms, treatment effects, and quality of life are accurately captured and reported. Effective communication and project management skills are essential, as PRO specialists play a key role in translating patient feedback into actionable insights that inform clinical decision-making and regulatory submissions.

What are the key skills and qualifications needed to thrive as a patient reported outcomes specialist, and why are they important?

To thrive as a Patient Reported Outcomes (PRO) Specialist, you typically need a background in healthcare, life sciences, or public health, with expertise in data collection, analysis, and research methodologies related to patient experiences. Familiarity with statistical software (such as SAS or SPSS), electronic PRO (ePRO) systems, and regulatory guidelines is often required. Excellent communication, critical thinking, and project management skills help you collaborate effectively with cross-functional teams and interpret patient data accurately. These skills are crucial to ensure that patient perspectives inform healthcare decisions, enhance clinical research, and support regulatory submissions.

What is the difference between Patient Reported Outcomes vs Clinical Data Analysts?

AspectPatient Reported OutcomesClinical Data Analysts
CredentialsTypically require healthcare or research background, often with degrees in health sciences or related fieldsRequire strong statistical, analytical, and data management skills, often with degrees in statistics, data science, or related fields
Work EnvironmentHealthcare settings, research institutions, or clinical trial environmentsHospitals, research organizations, pharmaceutical companies, or healthcare analytics firms
Employer & Industry UsageUsed to gather patient perspectives on health status and treatment outcomesAnalyze clinical data to support research, regulatory submissions, and healthcare decision-making

While Patient Reported Outcomes focus on collecting patient perspectives on health and treatment effects, Clinical Data Analysts interpret and analyze clinical data to support research and healthcare decisions. Both roles are vital in healthcare but serve different functions in improving patient care and advancing medical research.

What are popular job titles related to Patient Reported Outcomes jobs in Florida?

For Patient Reported Outcomes jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Patient Reported Outcomes jobs in Florida look for?

The top searched job categories for Patient Reported Outcomes jobs in Florida are:

Patient Reported Outcomes jobs near you
Infographic showing various Patient Reported Outcomes job openings in Florida as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution.

Clinical Research Coordinator 1

The University of Miami

Miami, FL • On-site

$23.25 - $30.75/hr

Full-time

Medical, Dental

Re-posted 22 days ago

University Of Miami rating

7.7

Company rating: 7.7 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

265th of 629 rated colleges and universities

Job description

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 department of Medicine has an exciting opportunity for a full-time Clinical Research Coordinator 1 to work onsite on the UHealth campus. This full-time position, Clinical Research Coordinator 1 (hereafter, "Coordinator"), will support two ongoing research programs within the University of Miami Division of Infectious Diseases: the Centers for AIDS Research Network of Integrated Clinical Systems (CNICS) cohort and the ADELANTE clinical research study. Both projects are conducted within an HIV clinical care setting and involve direct interaction with adults living with HIV. The Coordinator will perform a variety of patient-facing clinical research activities while working closely with investigators, clinicians, research staff, and community partners to ensure successful study implementation and participant retention.
CORE RESPONSIBILITIES
  • Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols.
  • Maintains enrollment procedures according to the protocol.
  • Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation.
  • Performs moderate to complex research tests/ experiments and adapts procedures for quality improvement under supervision.
  • Understands and follows technical instructions for operating clinical research equipment, problem solves when operational failures occur.
  • Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants.
  • Addresses adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study.
  • Identifies, reports, and helps problem solve protocol deviations and unanticipated occurrences.
  • Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
  • Knows the contents and maintenance of study-specific clinical research regulatory binders.
  • Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
  • Adheres to University and unit-level policies and procedures and safeguards University assets.

Department Specific Functions
  • Conducts participant recruitment and screening activities within the HIV clinic and through telephone outreach to identify potentially eligible participants.
  • Explains research studies to prospective participants, obtains informed consent, and answers participant questions while maintaining ethical standards and participant confidentiality.
  • Coordinates study visits by scheduling participant appointments and collaborating with clinic providers and research staff to facilitate research activities.
  • Collects research data through interviews, questionnaires, electronic patient-reported outcomes, and other study-specific assessments.
  • Performs chart review and medical record abstraction to support participant eligibility, study documentation, and data collection.
  • Maintains accurate and timely study documentation, case report forms, source documents, enrollment logs, and regulatory records in accordance with study protocols and institutional requirements.
  • Enters research data into electronic databases and assists with data quality assurance activities.
  • Assists with the collection, labeling, processing, storage, and shipment of clinical specimens according to protocol and institutional procedures.
  • Coordinates participant reimbursement and maintains documentation related to participant payments.
  • Contacts participants by telephone, text message, email, or other approved methods to schedule visits, complete follow-up assessments, and promote participant retention.
  • Works closely with investigators, clinic personnel, and collaborating research teams to ensure timely completion of study activities and protocol requirements.
  • Assists with reporting adverse events, protocol deviations, and other study-related issues to the Principal Investigator and research leadership, following applicable regulatory requirements.
  • Participates in study team meetings, trainings, and quality improvement activities.
  • Supports research activities within the HIV clinic while providing professional, culturally sensitive, and participant-centered interactions.
  • Assists with additional clinical research activities as assigned in support of the CNICS cohort, the ADELANTE study, and other related research initiatives within the Miami CFAR Behavioral & Social Sciences Community Outreach Core

This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.
CORE REQUIREMENTS
  • Bachelor's degree in relevant field required
  • Minimum 1 year of relevant experience
  • Bilingual proficiency in English and Spanish is highly desirable, as a significant proportion of study participants are Spanish speaking

Knowledge, Skills and Attitudes:
  • Skill in completing assignments accurately and with attention to detail.
  • Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
  • Ability to process and handle confidential information with discretion.
  • 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.

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 ground breaking 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

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About University of Miami

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The University of Miami, located in the beautiful Coral Gables, Florida, is a comprehensive, private research institution in the United States. Operating within the higher education industry, the institution offers a multitude of degree programs spanning over 180 majors and program through its 12 colleges. The University was founded in 1925 with the mission to disseminate knowledge, transform lives, and change the world - a mission it has held faithfully to this day. Notably, the University of Miami has gained global recognition for its commitment to research and innovation, with over $324 million in research and sponsored project funding awarded annually.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Coral Gables, FL, US

Year founded

1925

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