Clinical Research Visa Sponsorship Jobs in Florida
Florida is one of the most active states for clinical research hiring, anchored by major academic medical centers and life sciences employers across Miami, Orlando, and Tampa. Organizations like the University of Miami Health System, AdventHealth, and Moffitt Cancer Center regularly hire for research roles and have sponsored international candidates for work visas.
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Get Access To All JobsINTRODUCTION
The University of Miami, College of Arts and Sciences, has an exciting opportunity for a full time Clinical Research Coordinator 1 to work in Coral Gables, FL. The Department of Psychology and the Sylvester Comprehensive Cancer Center have a new opportunity for a full-time Clinical Research Coordinator 1 to assist research projects focused on developing and testing patient-centered behavioral strategies to improve health and wellbeing in the context of cancer. This role provides an excellent opportunity for those interested in behavioral health and non-pharmacologic intervention trials in healthcare settings. The Clinical Research Coordinator 1 will have a foundation in clinical research through assigned responsibilities in data management and implementing clinical research protocols. This role assumes responsibility for clinical research protocols and timelines including the planning, coordinating, implementing, and monitoring of clinical research studies. The incumbent works closely with study team members, clinicians, study patients, and other study sites, and operates with the goal of advancing their expertise through continued education, training, and research.
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
This position offers unique opportunities to learn about behavioral treatments and strategies and digital health interventions for promoting health behaviors, self-efficacy, and quality of life among adult patients in the context of cancer. The incumbent will work under the supervision of study investigators. As part of this role, additional opportunities may include assisting the study investigators with scholarly tasks including the preparation of scientific abstracts; conducting literature reviews and synthesizing relevant data; and conducting participant interviews.
CORE QUALIFICATIONS
- Bachelor’s degree in relevant field required
- Minimum 1 year of relevant experience required
- 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.
JOB STATUS
Full time
EMPLOYEE TYPE
Staff
The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here for additional information.
INTRODUCTION
The University of Miami, College of Arts and Sciences, has an exciting opportunity for a full time Clinical Research Coordinator 1 to work in Coral Gables, FL. The Department of Psychology and the Sylvester Comprehensive Cancer Center have a new opportunity for a full-time Clinical Research Coordinator 1 to assist research projects focused on developing and testing patient-centered behavioral strategies to improve health and wellbeing in the context of cancer. This role provides an excellent opportunity for those interested in behavioral health and non-pharmacologic intervention trials in healthcare settings. The Clinical Research Coordinator 1 will have a foundation in clinical research through assigned responsibilities in data management and implementing clinical research protocols. This role assumes responsibility for clinical research protocols and timelines including the planning, coordinating, implementing, and monitoring of clinical research studies. The incumbent works closely with study team members, clinicians, study patients, and other study sites, and operates with the goal of advancing their expertise through continued education, training, and research.
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
This position offers unique opportunities to learn about behavioral treatments and strategies and digital health interventions for promoting health behaviors, self-efficacy, and quality of life among adult patients in the context of cancer. The incumbent will work under the supervision of study investigators. As part of this role, additional opportunities may include assisting the study investigators with scholarly tasks including the preparation of scientific abstracts; conducting literature reviews and synthesizing relevant data; and conducting participant interviews.
CORE QUALIFICATIONS
- Bachelor’s degree in relevant field required
- Minimum 1 year of relevant experience required
- 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.
JOB STATUS
Full time
EMPLOYEE TYPE
Staff
The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here for additional information.
Clinical Research Job Roles in Florida
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Search Clinical Research Jobs in FloridaClinical Research Jobs in Florida: Frequently Asked Questions
Which companies sponsor visas for clinical research roles in Florida?
Florida's largest clinical research visa sponsors include Moffitt Cancer Center, the University of Miami Health System, AdventHealth, Tampa General Hospital, and Mayo Clinic's Florida campus. Contract research organizations with Florida offices, including ICON and Labcorp Drug Development, have also sponsored clinical research coordinators and associates. Academic medical centers tend to have established immigration processes and sponsor H-1B visa and O-1 visa petitions with some regularity.
Which visa types are most common for clinical research roles in Florida?
The H-1B is the most common visa category for clinical research coordinators, research scientists, and clinical data managers in Florida, as these roles typically require a relevant bachelor's degree or higher. Candidates with advanced degrees may also qualify for the EB-2 National Interest Waiver if their research has broader public health implications. J-1 visas are sometimes used for research fellows at academic institutions, though they may carry a two-year home residency requirement.
Which cities in Florida have the most clinical research sponsorship jobs?
Miami leads Florida for clinical research sponsorship activity, driven by the University of Miami Miller School of Medicine and a concentration of hospital networks. Orlando is a growing hub, with AdventHealth and UCF Health anchoring research hiring. Tampa has significant activity through Moffitt Cancer Center, Tampa General, and the University of South Florida Health. Jacksonville, home to Mayo Clinic's Southeast campus, is also a consistent source of sponsored clinical research positions.
How to find clinical research visa sponsorship jobs in Florida?
Migrate Mate filters job listings specifically for roles where employers have a documented history of visa sponsorship, making it easier to identify clinical research positions in Florida without sorting through postings that won't support international candidates. You can filter by state and role type to surface openings at Florida hospitals, academic medical centers, and contract research organizations. Searching for titles like clinical research coordinator, clinical research associate, and clinical data manager on Migrate Mate will return the most relevant Florida-specific results.
Are there any Florida-specific considerations for international clinical research job seekers?
Florida's large academic medical system creates a meaningful pipeline for international hires, particularly candidates with graduate training in clinical research, public health, or biomedical sciences from Florida universities. Employers in Florida are subject to federal H-1B prevailing wage requirements set by the Department of Labor, which are calibrated to local wage levels and vary between Miami, Tampa, and Orlando metro areas. Research roles tied to NIH-funded projects at state universities may have more structured sponsorship processes than private employers.
What is the prevailing wage for sponsored clinical research jobs in Florida?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.