Clinical Research Associate Visa Sponsorship Jobs in Florida
Florida is one of the most active states for clinical research associate roles, driven by major research hospitals, pharmaceutical companies, and CROs concentrated in Tampa, Miami, and Orlando. Employers like Novartis, Pfizer, PPD, ICON, and the University of Florida Health system regularly hire CRAs and have established visa sponsorship programs for qualified international candidates.
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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 Associate Job Roles in Florida
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Search Clinical Research Associate Jobs in FloridaClinical Research Associate Jobs in Florida: Frequently Asked Questions
Which companies sponsor visas for clinical research associates in Florida?
Contract research organizations with a significant Florida presence, including ICON, PPD, Syneos Health, and PRA Health Sciences, have consistent histories of sponsoring H-1B and other work visas for CRA roles. Large academic medical centers such as University of Florida Health, Tampa General Hospital, and Miami's Jackson Health System also sponsor international hires for clinical research positions, as do pharmaceutical sponsors with Florida operations.
Which visa types are most common for clinical research associate roles in Florida?
The H-1B is the most common visa category for clinical research associates in Florida, as the role typically qualifies as a specialty occupation requiring a bachelor's degree or higher in a life sciences field. International candidates with Canadian or Mexican citizenship may qualify for the TN visa under the NAFTA/USMCA professional categories. Australians may be eligible for the E-3 visa. OPT and STEM OPT are also widely used by recent graduates before employer-sponsored petitions.
Which cities in Florida have the most clinical research associate sponsorship jobs?
Tampa and the surrounding Bay Area represent Florida's largest concentration of CRA sponsorship activity, anchored by Moffitt Cancer Center, BayCare Health, and multiple CRO offices. Miami follows closely, supported by a dense network of hospitals and biotech firms conducting oncology and infectious disease trials. Orlando is a growing market, with AdventHealth and Nemours Children's Health driving clinical trial volume. Gainesville has consistent demand tied to the University of Florida's research enterprise.
How to find clinical research associate visa sponsorship jobs in Florida?
Migrate Mate is specifically built for international job seekers and filters clinical research associate openings in Florida by visa sponsorship eligibility, saving you from manually screening hundreds of postings. CRA roles in Florida are concentrated at CROs, academic medical centers, and pharmaceutical companies, and Migrate Mate surfaces verified sponsorship-active employers in the Tampa, Miami, and Orlando markets so you can focus your applications on companies that have actually sponsored visas for this role.
Are there any Florida-specific considerations for clinical research associates seeking visa sponsorship?
Florida's large population of clinical trial participants, particularly in oncology, cardiology, and infectious disease, means CRA demand tracks closely with trial enrollment volume at major research institutions. Employers filing H-1B petitions must pay the prevailing wage for CRA roles as determined by the Department of Labor for the specific Florida metropolitan area. Candidates with experience in FDA-regulated GCP environments and familiarity with therapeutic areas common in South Florida trials, such as HIV and tropical diseases, are particularly competitive.
What is the prevailing wage for sponsored clinical research associate 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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