Clinical Research Visa Sponsorship Jobs in Oklahoma
Oklahoma's clinical research sector is anchored by major academic medical centers and health systems including OU Health, INTEGRIS Health, and Hillcrest Medical Center, with Oklahoma City and Tulsa serving as the primary hiring hubs. International candidates with experience in clinical trials, regulatory affairs, or research coordination will find H-1B and TN sponsorship opportunities concentrated at these institutions.
See All Clinical Research JobsOverview
Showing 5 of 42+ Clinical Research Jobs in Oklahoma with Visa Sponsorship jobs
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
See all 42+ Clinical Research Jobs in Oklahoma with Visa Sponsorship
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Research Jobs in Oklahoma with Visa Sponsorship.
Get Access To All JobsJob Summary:
The Clinical Research Coordinator performs clinical research activities, investigations, and develops and compiles reports based on records, observations, test results and other information received for the purpose of advancing knowledge through clinical trial research in multiple disciplines. This role ensures timely and accurate reporting of adverse events, and helps maintain study budgets, supplies, and regulatory documentation.
Minimum Qualifications:
Bachelor’s degree, preferred.
Licensure, Registration and/or Certification:
Certified Clinical Research Professional (CCRP), preferred.
Work Experience:
Minimum 2 years of related experience in clinical research with a medical or scientific background.
Knowledge, Skills and Abilities:
- Comprehensive knowledge of medical terminology and current healthcare management methodology.
- Ability to use logical and/or scientific thinking to solve problems.
- Ability to follow and interpret written and verbal instructions.
- Ability to perform basic algebraic and geometric calculations as needed to compute dosage levels of drugs based on lab test results.
- Working knowledge of clinical research practices and protocols.
- Working knowledge of applicable guidelines and laws pursuant to clinical research.
- Ability to work in Word proficiently with working knowledge of Excel and Access or other database program used in the production of reports.
- Effective interpersonal, written, and verbal communication skills.
- Ability to organize and prioritize work in an effective and efficient manner.
- Ability to be detail oriented as required in the examination of clinical and numerical data.
Essential Functions and Responsibilities:
- Recruits and screens clinical research patients for protocol eligibility.
- Obtains informed consent through patient education; instructs patients regarding study design and purpose, anticipated side effects, patient's responsibilities and rights.
- Serves as a resource to physicians concerning protocol requirements and determines data requirements as delineated by each trial.
- Performs data collection and analysis of test results and records relating to clinical research.
- Collects appropriate data from physician offices and patient charts regarding research studies.
- Serves as liaison for patients, patient families, physicians, and regulatory body representatives for the purpose of providing a single point of contact for information, education and issue resolution.
- Coordinates with physician offices or treatment sites to assure billing compliance and drug accountability.
- Instructs the research data analyst to ensure that protocol parameters and treatment guidelines are correctly applied.
- Prepares new study applications, writes informed consent and submits for Institutional Research Ethics Board (IREB) approval according to applicable regulations.
Decision Making:
Independent judgment in making decisions involving non-routine problems under general supervision.
Working Relationships:
Coordinates activities of others (does not supervise). Leads others in same work performed (does not supervise). Works directly with patients and/or customers. Works with internal and/or external customers via telephone or face to face interaction. Works with other healthcare professionals and staff. Works frequently with individuals at Director level or above.
Special Job Dimensions:
None.
Supplemental Information:
This document generally describes the essential functions of the job and the physical demands required to perform the job. This compilation of essential functions and physical demands is not all inclusive nor does it prohibit the assignment of additional duties.
Location:
Tulsa, Oklahoma 74136
EOE Protected Veterans/Disability
Job Summary:
The Clinical Research Coordinator performs clinical research activities, investigations, and develops and compiles reports based on records, observations, test results and other information received for the purpose of advancing knowledge through clinical trial research in multiple disciplines. This role ensures timely and accurate reporting of adverse events, and helps maintain study budgets, supplies, and regulatory documentation.
Minimum Qualifications:
Bachelor’s degree, preferred.
Licensure, Registration and/or Certification:
Certified Clinical Research Professional (CCRP), preferred.
Work Experience:
Minimum 2 years of related experience in clinical research with a medical or scientific background.
Knowledge, Skills and Abilities:
- Comprehensive knowledge of medical terminology and current healthcare management methodology.
- Ability to use logical and/or scientific thinking to solve problems.
- Ability to follow and interpret written and verbal instructions.
- Ability to perform basic algebraic and geometric calculations as needed to compute dosage levels of drugs based on lab test results.
- Working knowledge of clinical research practices and protocols.
- Working knowledge of applicable guidelines and laws pursuant to clinical research.
- Ability to work in Word proficiently with working knowledge of Excel and Access or other database program used in the production of reports.
- Effective interpersonal, written, and verbal communication skills.
- Ability to organize and prioritize work in an effective and efficient manner.
- Ability to be detail oriented as required in the examination of clinical and numerical data.
Essential Functions and Responsibilities:
- Recruits and screens clinical research patients for protocol eligibility.
- Obtains informed consent through patient education; instructs patients regarding study design and purpose, anticipated side effects, patient's responsibilities and rights.
- Serves as a resource to physicians concerning protocol requirements and determines data requirements as delineated by each trial.
- Performs data collection and analysis of test results and records relating to clinical research.
- Collects appropriate data from physician offices and patient charts regarding research studies.
- Serves as liaison for patients, patient families, physicians, and regulatory body representatives for the purpose of providing a single point of contact for information, education and issue resolution.
- Coordinates with physician offices or treatment sites to assure billing compliance and drug accountability.
- Instructs the research data analyst to ensure that protocol parameters and treatment guidelines are correctly applied.
- Prepares new study applications, writes informed consent and submits for Institutional Research Ethics Board (IREB) approval according to applicable regulations.
Decision Making:
Independent judgment in making decisions involving non-routine problems under general supervision.
Working Relationships:
Coordinates activities of others (does not supervise). Leads others in same work performed (does not supervise). Works directly with patients and/or customers. Works with internal and/or external customers via telephone or face to face interaction. Works with other healthcare professionals and staff. Works frequently with individuals at Director level or above.
Special Job Dimensions:
None.
Supplemental Information:
This document generally describes the essential functions of the job and the physical demands required to perform the job. This compilation of essential functions and physical demands is not all inclusive nor does it prohibit the assignment of additional duties.
Location:
Tulsa, Oklahoma 74136
EOE Protected Veterans/Disability
Clinical Research Job Roles in Oklahoma
See all 42+ Clinical Research Jobs in Oklahoma
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Clinical Research Jobs in OklahomaClinical Research Jobs in Oklahoma: Frequently Asked Questions
Which companies sponsor visas for clinical research roles in Oklahoma?
The most active sponsors for clinical research positions in Oklahoma are large academic medical centers and health systems, including OU Health (University of Oklahoma Health Sciences Center), INTEGRIS Health, Saint Francis Health System, and Hillcrest Medical Center. Pharmaceutical contract research organizations with Oklahoma operations also file H-1B petitions for roles such as clinical research associate and data manager. Sponsorship is concentrated in organizations with dedicated research divisions.
Which visa types are most common for clinical research roles in Oklahoma?
The H-1B is the most commonly sponsored visa for clinical research professionals in Oklahoma, covering roles like clinical research coordinator, clinical data manager, and regulatory affairs specialist, which are typically classified as specialty occupations requiring a relevant bachelor's degree or higher. Canadian and Mexican nationals may qualify for TN status under the NAFTA/USMCA scientific professional categories. Researchers affiliated with universities may also encounter J-1 exchange visitor sponsorship for specific fellowship or postdoctoral arrangements.
Which cities in Oklahoma have the most clinical research sponsorship jobs?
Oklahoma City is the dominant hub for clinical research sponsorship, driven by the University of Oklahoma Health Sciences Center campus and the surrounding medical corridor. Tulsa is the secondary market, with Saint Francis Health System and Hillcrest Medical Center running active clinical trial programs. Smaller research activity exists in Norman, tied to the main OU campus. Candidates targeting Oklahoma sponsorship should prioritize Oklahoma City and Tulsa when filtering their job search.
How to find clinical research visa sponsorship jobs in Oklahoma?
Migrate Mate filters clinical research job listings specifically by visa sponsorship availability, so you can browse Oklahoma openings without sorting through roles that won't support international candidates. Search for titles like clinical research coordinator, CRA, clinical data manager, or regulatory affairs specialist and filter to Oklahoma. Because sponsorship for clinical research roles in Oklahoma is concentrated at academic medical centers and health systems, focusing on those employer types on Migrate Mate will surface the most relevant opportunities.
Are there state-specific factors that affect clinical research visa sponsorship in Oklahoma?
Oklahoma's clinical research hiring is heavily tied to the University of Oklahoma Health Sciences Center, which acts both as a direct employer and as a training pipeline supplying talent to regional health systems. Employers sponsoring H-1B workers in clinical research must meet Department of Labor prevailing wage requirements for the specific role and geographic area, which are determined by the Standard Occupational Classification assigned to the position. International candidates with graduate-level training in life sciences, public health, or biostatistics tend to have the strongest alignment with available sponsored roles.
What is the prevailing wage for sponsored clinical research jobs in Oklahoma?
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.
See which clinical research employers are hiring and sponsoring visas in Oklahoma right now.
Search Clinical Research Jobs in Oklahoma