Clinical Research Visa Sponsorship Jobs in North Carolina
North Carolina's clinical research sector is anchored by the Research Triangle Park area, home to major employers like Syneos Health, Parexel, and Labcorp Drug Development, alongside Duke University Health System and UNC Health. International candidates with backgrounds in clinical operations, data management, or regulatory affairs will find meaningful visa sponsorship activity concentrated in this region.
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Get Access To All JobsINTRODUCTION
Our FSP team is currently seeking a Unblinded Sr. CRA 1 with 3+ years of monitoring! Candidates must reside within the United States.
WHAT YOU WILL DO
You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.
Responsibilities:
- Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned
- Responsible for all aspects of site management as prescribed in the project plans
- General On-Site Monitoring
- Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
- Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
- Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data
- Responsible for all aspects of registry management as prescribed in the project plans
- Undertake feasibility work when requested
- Complete Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
- Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
- Assist with training of new employees, e.g. co-monitoring
- Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned
- Perform other duties as assigned by management
Requirements
- University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
- 4+ years of Clinical Monitoring experience
- 50-60% overnight travel
The important thing for us is you are comfortable working in an environment that is:
- Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even a few minutes will create a quality issue.
- Changing priorities constantly asking you to prioritize and adapt on the spot.
- Teamwork and people skills are essential for the study to run smoothly.
- Technology based. We collect our data directly into an electronic environment.
Work Environment:
- Work is performed in an office environment with exposure to electrical office equipment.
- Frequent travel to clients/site locations with occasional travel both domestic and international.
Physical Requirements:
- Ability to sit for extended periods and operate a vehicle safely.
- Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
- Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
- Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
- Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
- Regular and consistent attendance.
- Varied hours may be required.
Target Pay Range: $125 - $132K
Applications will be accepted on an ongoing basis.
Learn more about our EEO & Accommodations request here.
INTRODUCTION
Our FSP team is currently seeking a Unblinded Sr. CRA 1 with 3+ years of monitoring! Candidates must reside within the United States.
WHAT YOU WILL DO
You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.
Responsibilities:
- Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned
- Responsible for all aspects of site management as prescribed in the project plans
- General On-Site Monitoring
- Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
- Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
- Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data
- Responsible for all aspects of registry management as prescribed in the project plans
- Undertake feasibility work when requested
- Complete Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
- Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
- Assist with training of new employees, e.g. co-monitoring
- Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned
- Perform other duties as assigned by management
Requirements
- University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
- 4+ years of Clinical Monitoring experience
- 50-60% overnight travel
The important thing for us is you are comfortable working in an environment that is:
- Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even a few minutes will create a quality issue.
- Changing priorities constantly asking you to prioritize and adapt on the spot.
- Teamwork and people skills are essential for the study to run smoothly.
- Technology based. We collect our data directly into an electronic environment.
Work Environment:
- Work is performed in an office environment with exposure to electrical office equipment.
- Frequent travel to clients/site locations with occasional travel both domestic and international.
Physical Requirements:
- Ability to sit for extended periods and operate a vehicle safely.
- Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
- Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
- Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
- Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
- Regular and consistent attendance.
- Varied hours may be required.
Target Pay Range: $125 - $132K
Applications will be accepted on an ongoing basis.
Learn more about our EEO & Accommodations request here.
Clinical Research Job Roles in North Carolina
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Search Clinical Research Jobs in North CarolinaClinical Research Jobs in North Carolina: Frequently Asked Questions
Which companies sponsor visas for clinical researchers in North Carolina?
Contract research organizations based in or near Research Triangle Park are among the most active sponsors, including Syneos Health, Parexel, and Labcorp Drug Development. Academic medical centers such as Duke University Health System and UNC Health also sponsor visa petitions for clinical research coordinators and associates. Large pharmaceutical companies with North Carolina operations, including Biogen and Novo Nordisk, have documented sponsorship histories as well.
Which visa types are most common for clinical research roles in North Carolina?
The H-1B visa is the most widely used visa for clinical research positions in North Carolina, particularly for roles requiring a bachelor's or advanced degree in a health science, life science, or related field. Candidates already holding F-1 OPT or STEM OPT authorization frequently transition into H-1B visa sponsorship. Some research-focused positions at academic institutions may also qualify for J-1 visa exchange visitor status under an authorized program.
Which cities in North Carolina have the most clinical research sponsorship jobs?
The Research Triangle area, encompassing Raleigh, Durham, and Chapel Hill, accounts for the largest share of clinical research sponsorship activity in North Carolina. This concentration reflects the presence of major CROs, pharmaceutical companies, and research universities in that corridor. Charlotte has a smaller but growing presence through hospital systems and emerging biotech. Outside these metros, significant sponsorship opportunities are limited.
How to find clinical research visa sponsorship jobs in North Carolina?
Migrate Mate is built specifically for international job seekers and filters clinical research roles by visa sponsorship status and location, making it straightforward to identify open positions in North Carolina. Rather than sorting through thousands of unfiltered postings, you can browse roles already confirmed to involve sponsorship activity from employers in the Research Triangle and beyond. Creating a profile lets you track new postings as they appear.
Are there state-specific factors that affect clinical research sponsorship in North Carolina?
North Carolina's concentration of CROs and academic research institutions in the Research Triangle creates a relatively active sponsorship market compared to most states, which benefits international applicants. UNC Chapel Hill, Duke, and NC State supply a pipeline of candidates and maintain relationships with sponsors. Employers filing H-1B petitions must meet Department of Labor prevailing wage requirements specific to the Raleigh-Durham and Charlotte metropolitan areas, which differ from national averages.
What is the prevailing wage for sponsored clinical research jobs in North Carolina?
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.