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
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory.
Job Overview:
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Key Responsibilities:
- Perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
Essential Functions
- If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
QUALIFICATIONS
- Bachelor's Degree in scientific discipline or health care preferred.
- Requires at least 2 years of on-site monitoring experience.
- Equivalent combination of education, training and experience may be accepted in lieu of degree.
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
- Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Good therapeutic and protocol knowledge as provided in company training.
COMPENSATION
The potential base pay range for this role, when annualized, is $101,600.00 - $169,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
LOCATION
Tampa, United States of America | Full time | Field-based | R1537588
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
INTRODUCTION
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory.
Job Overview:
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Key Responsibilities:
- Perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
Essential Functions
- If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
QUALIFICATIONS
- Bachelor's Degree in scientific discipline or health care preferred.
- Requires at least 2 years of on-site monitoring experience.
- Equivalent combination of education, training and experience may be accepted in lieu of degree.
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
- Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Good therapeutic and protocol knowledge as provided in company training.
COMPENSATION
The potential base pay range for this role, when annualized, is $101,600.00 - $169,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
LOCATION
Tampa, United States of America | Full time | Field-based | R1537588
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
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 and O-1 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.
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