Clinical Research Visa Sponsorship Jobs in West Virginia
Clinical research visa sponsorship jobs in West Virginia are concentrated around academic medical centers and health systems, particularly West Virginia University Health System in Morgantown and Charleston Area Medical Center. The state's growing focus on population health and rural clinical trials creates demand for research coordinators, data managers, and clinical trial specialists with specialized credentials.
Find Clinical Research JobsOverview
Showing 2 of 48+ Clinical Research Jobs in West Virginia with Visa Sponsorship




See all 48+ Clinical Research Jobs in West Virginia with Visa Sponsorship
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Research Jobs in West Virginia with Visa Sponsorship.
Get Access To All Jobs
INTRODUCTION
The Clinical Research Unit within the Cancer Institute at West Virginia University is currently accepting applications for a (Hybrid) Oncology Clinical Research Specialist.
About the Opportunity
The Clinical Research Coordinator III supports clinical trials (Phases I–IV) at the WVU Cancer Institute by coordinating research activities, ensuring protocol compliance, managing patient care, and maintaining data integrity. The role requires independent judgment, collaboration, and adherence to regulatory standards.
We strongly believe in work-life balance and keeping time for things we love outside our work. WVU offers generous benefits, including:
- 37.5-hour work week
- 13 paid holidays (staff holiday calendar)
- 24 annual leave (vacation) days per year (employee leave)
- 18 sick days per year (for when you’re ill, for when you need time to care for sick family, for your own, or your family’s, regularly scheduled medical appointments. Who is family for the purpose of this leave? A lot of people in your life including immediate relatives and in-laws as well as others considered to be members of your household living under the same roof)
- WVU offers a range of health insurance and other benefits
- 401(a) retirement savings with 6% employee contribution match, eligibility to continue health insurance, and other retiree perks. Looking for more retirement benefits information? Check out retirement health insurance benefits, retirement income, and FAQ’s.
- Wellness programs
- Protocol Conduct and Compliance - 30%
- Ensure compliance with current regulations, guidance and policies at the institutional, state, federal, and international levels.
- Assess feasibility of implementing new protocols.
- Collaborate with investigators, research staff, pharmacy, clinical staff and other ancillary departments to implement and conduct trials.
- Facilitate and participate in monitoring or auditing reviews conducted by internal and/or external agencies such as the U.S. Food and Drug Administration, industry, IRB and quality assurance.
- Serve as a liaison between the research team, clinical staff, and sponsors.
- Provide education to staff prior to implementation and throughout the lifecycle of the research study and monitor protocol adherence.
- Support community outreach and trial advocacy.
-
Collaborate with research team utilizing internal and external resources to develop a recruitment strategy for each research study and evaluate effectiveness.
-
Management of Clinical Trial Patients - 30%
- Ensure the initial and ongoing consent process is performed and documented in compliance with all applicable regulations, guidelines and policies.
- Educate patients on trial participation, providing updates and information throughout the lifecycle of the study.
- Assess for barriers to effective informed consent discussion and implement a plan to overcome as barriers are identified.
- Assess eligibility and monitor patient adherence.
- Ensure scheduling and adherence to all protocol tests and procedures.
- Perform study assessments and/or procedures within the employee’s scope of practice which may include but not limited to vital signs, ECG, administering questionnaires, etc.
- Assess and document adverse events in collaboration with the investigator.
- Collaborate with investigator on dose modifications and treatment responses.
-
Advocate for ethical care of participants while adhering to the protocol requirements.
-
Documentation and Training - 20%
- Maintain accurate source documentation and data reporting.
- Provide protocol training to clinical staff and/or other members of the research team.
- Ensure proper documentation practices from clinical staff and provide additional training, as needed.
-
Update the Clinical Trial Management System (CTMS) with protocol and patient information.
-
Financial Stewardship - 10%
- Review trial budgets and coverage analyses for adequacy of funding.
- Distinguish between routine care and research-related expenses.
-
Ensure patients are reimbursed for research related expenses and/or stipends provided per protocol/contract.
-
Professional Development and Leadership - 10%
- Participates in educational opportunities to increase knowledge about oncology and clinical research.
- May lead projects or coordinate team efforts.
- Assist with onboarding and training research staff.
Qualifications
- Bachelor's degree from an allied health discipline, or related medical field (such as nursing, medical technology, pharmacy, etc.)
- A minimum of two (2) years of experience in the following:
- Working in a clinical setting and/or experience in clinical research
- Any equivalent combination of related education and/or experience will be considered.
- All qualifications must be met by the time of employment.
Knowledge, Skills, and Abilities
- Knowledge of clinical trials research.
- Must possess and apply knowledge of many different and unrelated processes and methods related to such areas as:
- Patient care – information and techniques needed to diagnose and treat human injuries, diseases, and deformities. This includes symptoms, treatment alternatives, drug properties and interactions, and preventive health-care measures.
- Treatment design, administration and modification.
- Counseling and education – principles and methods for training design, teaching and instruction for individuals and groups, and the measurement of training effects.
- Data collection, validation, entry, analysis, and reporting.
- Human subjects protection and related issues – knowledge of professional principles (GCP and IRB guidelines), legal and/or reporting requirements affecting grants and contracts, and adheres to industry and government standards.
- Skilled at being aware of others’ reactions and understanding why they react as they do.
- Skilled at communicating effectively in writing as appropriate for the needs of the audience.
- Skilled at using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions, or approached to problems.
- Knowledge of principles and processes for providing customer and personal services. This includes customer needs assessment, meeting quality standards for services, and evaluation of customer satisfaction.
- Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public. Position requires excellent customer service skills and the ability to communicate effectively with patients and families; pharmaceutical company personnel; regulatory and monitoring agency personnel; and, internal staff members. Communicates with physicians, patients, students and employees of WVU, WVU Hospitals, MBRCC and UHA.
- Ability to develop constructive and cooperative working relationships with others and maintain them over time.
- Ability to read, analyze and interpret general business periodicals, professional journals, technical procedures or governmental regulations.
- Ability to write reports, business correspondence, and procedure manuals.
- Ability to arrange things or actions in a certain order or pattern according to a specific rule or set of rules (e.g., patterns of numbers, letters, words, pictures, mathematical operations).
- Ability to combine pieces of information to form general rules or conclusions (includes finding a relationship among seemingly unrelated events).
- Ability to analyze information and evaluate results to choose the best solution, solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.
- Ability to interpret a variety of instructions furnished in written, oral, diagram or schedule form.
- Ability to develop specific goals and plans, to prioritize, organize and accomplish tasks independently and through others.
Requirements
- If applicable, valid RN license from the State of West Virginia.
About WVU
West Virginia University is a place of purpose and community. We take pride in our profound impact on the state of West Virginia and are committed to the personal and professional growth of our employees.
From the groundbreaking R1 research at our flagship campus in Morgantown to the career-oriented programs at WVU Potomac State in Keyser, and the technology-intensive programs at WVU Tech in Beckley, the contributions of WVU employees resonate across the state, touching lives and shaping futures.
At WVU, you will discover a supportive community that champions work-life balance and fosters a collaborative atmosphere. Our core values — service, curiosity, respect, accountability and appreciation — unite us as Mountaineers.
Join us at West Virginia University, where your work will make a lasting impact. To learn more about WVU, visit wvu.edu.
West Virginia University is an Equal Opportunity Employer. We invite all qualified applicants regardless of race, color, religion, sex, national origin, age, disability, genetic information, or Veteran status.
Job Posting
: Sep 11, 2026
Posting Classification: Non-Classified
Exemption Status: Exempt
Benefits Eligible: Yes
Schedule
: Full-time
Clinical Research Job Roles in West Virginia
See all 48+ Clinical Research Jobs in West Virginia
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Clinical Research Jobs in West VirginiaClinical Research Jobs in West Virginia: Frequently Asked Questions
Which companies sponsor visas for clinical research professionals in West Virginia?
West Virginia University Health System is the state's most active sponsor for clinical research roles, operating through WVU Medicine and its affiliated research institutes. Charleston Area Medical Center and the WVU Cancer Institute also have histories of sponsoring international researchers. Academic medical centers and federally funded research programs within the state are generally the most consistent sources of visa sponsorship for clinical research positions.
Which visa types are most common for clinical research roles in West Virginia?
The H-1B visa is the most common visa for clinical research coordinators, data managers, and research scientists in West Virginia, as these roles typically require at least a bachelor's degree in a qualifying specialty field. J-1 visas appear frequently for postdoctoral research fellows hosted through WVU. Candidates with advanced degrees in life sciences, biostatistics, or epidemiology may also explore the EB-2 immigrant visa pathway through employer sponsorship.
Which cities in West Virginia have the most clinical research sponsorship jobs?
Morgantown is the clear center of clinical research activity in West Virginia, driven by West Virginia University and WVU Medicine, which house multiple research centers and clinical trial units. Charleston is the secondary hub, with Charleston Area Medical Center conducting sponsored trials. Huntington, home to Marshall University and its Joan C. Edwards School of Medicine, also generates a smaller but consistent set of research-related openings.
How to find clinical research visa sponsorship jobs in West Virginia?
Migrate Mate filters clinical research jobs in West Virginia specifically by visa sponsorship availability, saving you the time of screening postings manually. The platform surfaces roles at employers like WVU Medicine and other health systems that have documented sponsorship histories. Because West Virginia's clinical research market is smaller than coastal states, setting up alerts on Migrate Mate for new postings helps you respond quickly when relevant roles open.
Are there state-specific considerations for clinical research visa sponsorship in West Virginia?
West Virginia's clinical research sector is heavily tied to federal grant funding through the NIH COBRE and IDeA programs, which support infrastructure at WVU and Marshall University. Roles funded through federal grants often have stable, multi-year hiring cycles. The state's rural health focus means clinical trial experience in underserved population research is a differentiating credential. Employers must still meet Department of Labor prevailing wage requirements when sponsoring H-1B workers, regardless of the state's generally lower cost of living.
What is the prevailing wage for sponsored clinical research jobs in West Virginia?
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.