Clinical Specialist Visa Sponsorship Jobs in Nebraska
Nebraska's clinical specialist jobs are concentrated in Omaha and Lincoln, where health systems like Nebraska Medicine, CHI Health, and Bryan Health regularly hire for device, pharmaceutical, and diagnostics roles. The state's growing medical device presence and proximity to major Midwest distribution hubs make it an active market for international clinical specialist candidates seeking visa sponsorship.
See All Clinical Specialist JobsOverview
Showing 5 of 32+ Clinical Specialist Jobs in Nebraska 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 32+ Clinical Specialist Jobs in Nebraska with Visa Sponsorship
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Specialist Jobs in Nebraska with Visa Sponsorship.
Get Access To All JobsINTRODUCTION
The Clinical Data Specialist is responsible for the review of all source data and ensure all applicable data is entered into its respective database and/or Case Report Form (CRF). Ensure the completeness, accuracy, and consistency of source data and CRF data entry so that it meets the standard of quality expected for reporting to Sponsors and regulatory bodies. Participate with auxiliary teams involved in study set up, conduct, and data cleaning of clinical trials. This is an entry level position that pays $21/hour.
ESSENTIAL FUNCTIONS:
- Attend study setup meetings to determine QC criteria and timelines for each study
- Review study-specific source documents to ensure all forms are accurate prior to study start and that all data collected is in accordance with study-specific Case Report Forms and protocol requirements.
- Ensure QC reviews are complete in accordance with study-specific timelines
- Review source data on an ongoing basis to ensure the following: Clinical source data is complete according to GCP and FDA guidelines, protocol deviations (if applicable) are documented, and source data is collected in accordance with Sponsor requirements, and Celerion SOPs/PGs.
- Ensure data corrections are completed according to GCP guidelines, and Celerion SOPs/PGs.
- Complete a Final QC to ensure all source data is accounted for and has been QC reviewed.
- Perform accurate data entry and verification for Celerion Standard and Sponsor Provided EDCs.
- Archive source documentation including CRFs.
- Complete QC/DE dedicated milestones in a timely manner.
- Perform standard quality control steps.
REQUIREMENTS
- High School Diploma or GED (relevant internal Celerion experience in lieu preferred).
- 1 - 2 years industry experience preferred.
- Previous Quality Control/ Data Entry or related experience preferred.
- Medical Terminology Training preferred.
- Excellent oral and written communication skills.
- Ability to organize and manage multiple priorities.
- Experience working in an environment with complex processes and defined criteria.
- Excellent time management skills required.
- Proficient in MS Office applications required.
- Excellent attention to detail skills required.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
INTRODUCTION
The Clinical Data Specialist is responsible for the review of all source data and ensure all applicable data is entered into its respective database and/or Case Report Form (CRF). Ensure the completeness, accuracy, and consistency of source data and CRF data entry so that it meets the standard of quality expected for reporting to Sponsors and regulatory bodies. Participate with auxiliary teams involved in study set up, conduct, and data cleaning of clinical trials. This is an entry level position that pays $21/hour.
ESSENTIAL FUNCTIONS:
- Attend study setup meetings to determine QC criteria and timelines for each study
- Review study-specific source documents to ensure all forms are accurate prior to study start and that all data collected is in accordance with study-specific Case Report Forms and protocol requirements.
- Ensure QC reviews are complete in accordance with study-specific timelines
- Review source data on an ongoing basis to ensure the following: Clinical source data is complete according to GCP and FDA guidelines, protocol deviations (if applicable) are documented, and source data is collected in accordance with Sponsor requirements, and Celerion SOPs/PGs.
- Ensure data corrections are completed according to GCP guidelines, and Celerion SOPs/PGs.
- Complete a Final QC to ensure all source data is accounted for and has been QC reviewed.
- Perform accurate data entry and verification for Celerion Standard and Sponsor Provided EDCs.
- Archive source documentation including CRFs.
- Complete QC/DE dedicated milestones in a timely manner.
- Perform standard quality control steps.
REQUIREMENTS
- High School Diploma or GED (relevant internal Celerion experience in lieu preferred).
- 1 - 2 years industry experience preferred.
- Previous Quality Control/ Data Entry or related experience preferred.
- Medical Terminology Training preferred.
- Excellent oral and written communication skills.
- Ability to organize and manage multiple priorities.
- Experience working in an environment with complex processes and defined criteria.
- Excellent time management skills required.
- Proficient in MS Office applications required.
- Excellent attention to detail skills required.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
Clinical Specialist Job Roles in Nebraska
See all 32+ Clinical Specialist Jobs in Nebraska
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Clinical Specialist Jobs in NebraskaClinical Specialist Jobs in Nebraska: Frequently Asked Questions
Which companies sponsor visas for clinical specialists in Nebraska?
Nebraska Medicine, CHI Health, and Bryan Medical Center are among the larger health systems in Nebraska that have sponsored work visas for clinical roles. On the medical device and diagnostics side, companies with regional sales and clinical support offices in Omaha, such as Medtronic and Abbott, have H-1B sponsorship histories. Sponsorship availability depends on the specific role, headcount, and hiring cycle, so verifying directly with each employer is important.
Which visa types are most common for clinical specialist roles in Nebraska?
The H-1B is the most common visa category for clinical specialist positions in Nebraska, particularly for roles requiring a bachelor's degree or higher in a clinical, biomedical, or life sciences field. Some candidates with advanced clinical degrees may also qualify under the O-1 for extraordinary ability. Clinical specialists employed by qualifying nonprofit health systems or academic medical centers, such as Nebraska Medicine, may access cap-exempt H-1B filings, which are not subject to the annual lottery.
Which cities in Nebraska have the most clinical specialist sponsorship jobs?
Omaha accounts for the majority of clinical specialist sponsorship activity in Nebraska, driven by its concentration of hospital systems, regional medical device offices, and diagnostics companies. Lincoln is the second-largest market, with opportunities tied to Bryan Health, the University of Nebraska Health System, and pharmaceutical support roles. Smaller markets like Kearney or Grand Island occasionally have openings but offer far fewer sponsored positions compared to the two metro areas.
How to find clinical specialist visa sponsorship jobs in Nebraska?
Migrate Mate is built specifically for international candidates and filters clinical specialist roles in Nebraska by visa sponsorship status, saving significant time compared to manually screening postings. You can browse current openings across Omaha, Lincoln, and other Nebraska locations to identify which employers are actively hiring and have a sponsorship history. Filtering by role type and location on Migrate Mate surfaces positions from health systems, medical device companies, and diagnostics firms operating across the state.
Are there any state-specific considerations for clinical specialists seeking sponsorship in Nebraska?
Nebraska's academic medical centers, particularly the University of Nebraska Medical Center in Omaha, serve as a meaningful pipeline for international clinical talent transitioning from training to sponsored employment. Employers filing H-1B petitions must meet the Department of Labor's prevailing wage requirements for the Omaha or Lincoln metropolitan areas, which are determined by the specific SOC code assigned to the clinical specialist role. Candidates should confirm that their job duties and educational background clearly support the specialty occupation classification required for H-1B eligibility.
What is the prevailing wage for sponsored clinical specialist jobs in Nebraska?
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 specialist employers are hiring and sponsoring visas in Nebraska right now.
Search Clinical Specialist Jobs in Nebraska