Principal Visa Sponsorship Jobs in Delaware
Principal visa sponsorship jobs in Delaware are concentrated in Wilmington, where financial services firms, law firms, and corporate headquarters cluster along the Brandywine Valley corridor. Employers including JPMorgan Chase, DuPont, and AstraZeneca have sponsored senior-level roles in the state. Delaware's corporate-friendly environment and proximity to Philadelphia expand the hiring pool for principal-level candidates.
Find Principal JobsOverview
Showing 5 of 111+ Principal Jobs in Delaware with Visa Sponsorship
See all 111+ Principal Jobs in Delaware with Visa Sponsorship
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Principal Jobs in Delaware with Visa Sponsorship.
Get Access To All JobsOverview:
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity.
Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
JOB SUMMARY (PRIMARY FUNCTION)
The Sr Principal, Biostatistical Programmer is responsible for processing clinical data required for statistical analysis of Phase I — III clinical trials and leading project teams.
ESSENTIAL FUNCTIONS OF THE JOB (KEY RESPONSIBILITIES)
- Conduct statistical programming work of clinical data using SAS Software.
- Ensure that all programs, outputs and documentation are consistent with ICH guidelines and are conducted in compliance with company SOPs.
- Generate analysis datasets according to CDISC standard and SAP.
- Implement analysis methods according to SAP, and produce summary tables, graphs and data listings using SAS; Conduct ad hoc analyses.
- Validate programs and associated results produced by other programming team members.
- Participate in TLF shell preparation and review, and assist statistician for SAP preparation.
- Run CDISC validation programs e.g. OpenCDISC reports to ensure ADaM datasets are CDISC compliant.
- Develop standard SAS macros for efficient analyses of clinical data under the guidance of Programming management.
- Participate in the review of 'Statistical Analysis Plan' and other documents essential to the conduct of statistical programming work for clinical trials.
- Collaborate with Clinical Research Organizations, as required, to participate in the oversight and management of programming activities to help ensure quality, timelines, and deliverables are met. Work independently to program for individual studies with minimal supervision.
- Function as a Lead programmer for a project or a group of studies performing the following functions:
- Maintain the overall timeline for their studies.
- Maintain the programming standards for their studies.
- Review standard macros used.
- Review standard datasets used.
- Discuss the need for programming resources for the group of studies.
- Guide and support team members on Incyte systems and standards as they work on studies within their area.
- Assist less experienced programmers in new study set-up to help identify similar studies.
- Review Production area after study programming is complete to make sure datasets, programs, and outputs are properly stored.
- Check that the validation summary reports are clean of errors and warnings, and show proper documentation of SAS programs.
- Review individual study CDISC validation output.
- Act as a Programming lead for a submission project under supervision of Programming management.
- Serve as a mentor to less experienced programmers and as an expert to provide recommendations and solutions to complex problems.
QUALIFICATIONS (MINIMAL ACCEPTABLE LEVEL OF EDUCATION, WORK EXPERIENCE, AND COMPETENCY)
- Discover – Develop – Deliver – Collaborate
- Strong organizational, time management, communication and project coordination and leadership skills.
- Demonstrate knowledge of regulatory guidelines, including electronic submission standards.
- Good SAS programming skills and attention to detail are essential.
- Experience with data management, including familiarity with CDISC standards, is highly desirable.
- Minimum of several years of programming experience using SAS/Base/Macro/GRAPH in the biopharmaceutical and/or CRO industries, or equivalent skills and knowledge.
- A degree in a relevant field such as statistics or computer sciences is preferred, but equivalent practical experience will also be considered.
- Demonstrate experience in mentoring team members and providing expert recommendations and solutions to complex problems.
- Must be able to manage multiple tasks while collaborating with team members effectively.
- Must be able to effectively manage workload and prioritize tasks in a dynamic environment.
Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
We Respect Your Privacy
The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.
During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job.
You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.
Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.
Overview:
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity.
Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
JOB SUMMARY (PRIMARY FUNCTION)
The Sr Principal, Biostatistical Programmer is responsible for processing clinical data required for statistical analysis of Phase I — III clinical trials and leading project teams.
ESSENTIAL FUNCTIONS OF THE JOB (KEY RESPONSIBILITIES)
- Conduct statistical programming work of clinical data using SAS Software.
- Ensure that all programs, outputs and documentation are consistent with ICH guidelines and are conducted in compliance with company SOPs.
- Generate analysis datasets according to CDISC standard and SAP.
- Implement analysis methods according to SAP, and produce summary tables, graphs and data listings using SAS; Conduct ad hoc analyses.
- Validate programs and associated results produced by other programming team members.
- Participate in TLF shell preparation and review, and assist statistician for SAP preparation.
- Run CDISC validation programs e.g. OpenCDISC reports to ensure ADaM datasets are CDISC compliant.
- Develop standard SAS macros for efficient analyses of clinical data under the guidance of Programming management.
- Participate in the review of 'Statistical Analysis Plan' and other documents essential to the conduct of statistical programming work for clinical trials.
- Collaborate with Clinical Research Organizations, as required, to participate in the oversight and management of programming activities to help ensure quality, timelines, and deliverables are met. Work independently to program for individual studies with minimal supervision.
- Function as a Lead programmer for a project or a group of studies performing the following functions:
- Maintain the overall timeline for their studies.
- Maintain the programming standards for their studies.
- Review standard macros used.
- Review standard datasets used.
- Discuss the need for programming resources for the group of studies.
- Guide and support team members on Incyte systems and standards as they work on studies within their area.
- Assist less experienced programmers in new study set-up to help identify similar studies.
- Review Production area after study programming is complete to make sure datasets, programs, and outputs are properly stored.
- Check that the validation summary reports are clean of errors and warnings, and show proper documentation of SAS programs.
- Review individual study CDISC validation output.
- Act as a Programming lead for a submission project under supervision of Programming management.
- Serve as a mentor to less experienced programmers and as an expert to provide recommendations and solutions to complex problems.
QUALIFICATIONS (MINIMAL ACCEPTABLE LEVEL OF EDUCATION, WORK EXPERIENCE, AND COMPETENCY)
- Discover – Develop – Deliver – Collaborate
- Strong organizational, time management, communication and project coordination and leadership skills.
- Demonstrate knowledge of regulatory guidelines, including electronic submission standards.
- Good SAS programming skills and attention to detail are essential.
- Experience with data management, including familiarity with CDISC standards, is highly desirable.
- Minimum of several years of programming experience using SAS/Base/Macro/GRAPH in the biopharmaceutical and/or CRO industries, or equivalent skills and knowledge.
- A degree in a relevant field such as statistics or computer sciences is preferred, but equivalent practical experience will also be considered.
- Demonstrate experience in mentoring team members and providing expert recommendations and solutions to complex problems.
- Must be able to manage multiple tasks while collaborating with team members effectively.
- Must be able to effectively manage workload and prioritize tasks in a dynamic environment.
Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
We Respect Your Privacy
The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.
During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job.
You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.
Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.
Principal Job Roles in Delaware
See all 111+ Principal Jobs in Delaware
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Principal Jobs in DelawarePrincipal Jobs in Delaware: Frequently Asked Questions
Which companies sponsor visas for principal roles in Delaware?
Delaware's largest visa sponsors for principal-level positions include financial institutions such as JPMorgan Chase and Bank of America, life sciences companies like AstraZeneca and Incyte, and corporate legal and consulting firms based in Wilmington. Delaware's status as the legal home of most U.S. corporations also means that law firms and registered agent companies regularly hire principals in specialized practice areas.
Which visa types are most common for principal roles in Delaware?
The H-1B visa is the most common visa for principal roles in Delaware, particularly in finance, law, consulting, and life sciences, where the specialty occupation requirement is clearly met by the degree-specific nature of the work. Senior professionals with extraordinary ability may qualify for the O-1A. Canadians and Mexicans in eligible professional categories may pursue TN visa status. Employers sponsoring permanent roles often move toward EB-2 or EB-3 immigrant petitions.
Which cities in Delaware have the most principal sponsorship jobs?
Wilmington accounts for the majority of principal sponsorship activity in Delaware, driven by its concentration of Fortune 500 corporate headquarters, major banks, and law firms. Newark, home to the University of Delaware, generates some demand through research and administrative principal roles. Dover, as the state capital, has a smaller but consistent presence in government-adjacent and healthcare-sector principal hiring.
How to find principal visa sponsorship jobs in Delaware?
Migrate Mate filters job listings specifically by visa sponsorship availability, making it straightforward to browse principal roles in Delaware without sorting through positions that don't support international candidates. Because principal titles span finance, law, life sciences, and technology, using Migrate Mate's role and location filters together helps narrow results to Delaware employers actively seeking sponsored candidates at this seniority level.
Are there state-specific considerations for principal-level sponsorship in Delaware?
Delaware's Department of Labor follows federal prevailing wage determinations for H-1B petitions, so there are no additional state wage floors beyond federal requirements. However, principal roles in Delaware's financial and legal sectors tend to sit at higher wage levels in the DOL's prevailing wage tiers, which affects the employer's LCA obligations. Delaware's small geographic size also means many employers treat the Wilmington metro as part of the broader Philadelphia labor market for wage determination purposes.
What is the prevailing wage for sponsored principal jobs in Delaware?
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.