Research Associate Visa Sponsorship Jobs in North Carolina
North Carolina's research associate positions are concentrated at Research Triangle Park institutions like Duke University, UNC-Chapel Hill, and NC State, alongside major pharmaceutical and biotech employers such as Biogen, Novo Nordisk, and GlaxoSmithKline. The Triangle, Charlotte's growing life sciences sector, and Raleigh's expanding tech corridor all generate steady demand for international research talent with visa sponsorship.
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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.
Research Associate Job Roles in North Carolina
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Search Research Associate Jobs in North CarolinaResearch Associate Jobs in North Carolina: Frequently Asked Questions
Which companies sponsor visas for research associates in North Carolina?
Major sponsors in North Carolina include Duke University, UNC-Chapel Hill, NC State University, RTI International, Biogen, Novo Nordisk, and GlaxoSmithKline. Large contract research organizations based in Research Triangle Park, such as Syneos Health and Labcorp, also have established sponsorship histories. University-affiliated medical centers and federally funded research institutes tend to be the most consistent sponsors for research associate roles.
Which visa types are most common for research associate roles in North Carolina?
The H-1B visa is the most common visa for research associate positions that require a specific bachelor's degree or higher in a relevant field, such as biology, chemistry, or biomedical science. Academic and nonprofit research institutions may also file under the H-1B cap-exempt pathway. F-1 OPT and STEM OPT extensions are frequently used by recent graduates before employer-sponsored petitions are filed.
Which cities in North Carolina have the most research associate sponsorship jobs?
The Research Triangle area, spanning Raleigh, Durham, and Chapel Hill, accounts for the largest share of research associate sponsorship jobs in the state. Research Triangle Park itself hosts dozens of pharmaceutical, biotech, and clinical research employers. Charlotte has a smaller but growing life sciences presence, and Greensboro and Winston-Salem offer additional opportunities tied to university medical research programs.
How to find research associate visa sponsorship jobs in North Carolina?
Migrate Mate filters job listings specifically by visa sponsorship eligibility, making it straightforward to browse research associate openings in North Carolina without sorting through employers that don't sponsor. You can narrow results by city or institution type to focus on the Triangle area, Charlotte, or academic medical centers. Migrate Mate's listings reflect employers with active sponsorship histories, which is particularly useful for research associate roles where sponsorship willingness varies widely by employer.
Are there any state-specific considerations for research associates pursuing visa sponsorship in North Carolina?
North Carolina's concentration of cap-exempt research institutions, including its major public universities and federally funded research centers, means some employers can file H-1B petitions outside the annual lottery. Research associates at nonprofits affiliated with higher education may benefit from this. The depth of the life sciences cluster in Research Triangle Park also means prevailing wage determinations are calibrated to a competitive regional market, which employers must meet when filing Labor Condition Applications.
What is the prevailing wage for sponsored research associate 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.