Clinical Research Associate Visa Sponsorship Jobs in Ohio
Ohio's clinical research associate market centers on Columbus, Cleveland, and Cincinnati, where major health systems like OhioHealth, Cleveland Clinic, and UC Health, alongside contract research organizations and pharmaceutical companies, regularly hire for CRA roles. International candidates with clinical trial monitoring experience and relevant science degrees will find active visa sponsorship opportunities across the state.
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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. Responsibilities 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
Cleveland, United States of America
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
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. Responsibilities 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
Cleveland, United States of America
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
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 Ohio
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Search Clinical Research Associate Jobs in OhioClinical Research Associate Jobs in Ohio: Frequently Asked Questions
Which companies sponsor visas for clinical research associates in Ohio?
Contract research organizations with Ohio operations, including ICON, Medpace (headquartered in Cincinnati), and Labcorp Drug Development, have sponsored H-1B visas for CRA roles. Major health systems such as Cleveland Clinic, OhioHealth, and the Ohio State University Wexner Medical Center also file sponsorship petitions for clinical research positions. Pharmaceutical and medical device companies with Midwest operations represent additional sponsoring employers worth targeting.
Which visa types are most common for clinical research associate roles in Ohio?
The H-1B is the most common visa category for clinical research associates in Ohio, as CRA positions typically qualify as specialty occupations requiring at least a bachelor's degree in a life science, nursing, or a related field. Candidates with a relevant master's or doctoral degree may also explore the EB-2 immigrant visa pathway. Some international candidates already in the U.S. on F-1 OPT or STEM OPT may use that work authorization while pursuing employer H-1B sponsorship.
Which cities in Ohio have the most clinical research associate sponsorship jobs?
Columbus leads in CRA sponsorship activity, driven by Ohio State University's clinical enterprise and a dense concentration of health systems and CROs. Cleveland ranks second, anchored by Cleveland Clinic and University Hospitals, both of which conduct extensive clinical trial programs. Cincinnati is a strong third, home to Medpace and UC Health. Smaller markets like Dayton and Toledo have more limited but still present sponsorship activity through regional hospital systems.
How to find clinical research associate visa sponsorship jobs in Ohio?
Migrate Mate filters job listings specifically for roles offering visa sponsorship, so you can search clinical research associate positions in Ohio without manually screening out employers who don't sponsor. The platform surfaces openings from CROs, health systems, and pharmaceutical companies across Columbus, Cleveland, and Cincinnati. Filtering by Ohio and the CRA role type on Migrate Mate narrows results to relevant sponsoring employers, which saves significant time in the job search process.
Are there state-specific considerations for clinical research associates seeking sponsorship in Ohio?
Ohio's strong university research infrastructure, particularly through Ohio State, Case Western Reserve, and the University of Cincinnati, creates a pipeline of clinical trial activity that sustains consistent CRA hiring. Employers sponsoring H-1B visas for CRA roles must meet DOL prevailing wage requirements for the Cincinnati, Columbus, or Cleveland metropolitan statistical areas, which vary by experience level and are set independently for each region. CROs in Ohio often prefer candidates with prior site monitoring experience and GCP certification, which can strengthen a sponsorship case.
What is the prevailing wage for sponsored clinical research associate jobs in Ohio?
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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