Biotech & Pharma H-1B Sponsorship Jobs in Georgia
Biotech and pharma H-1B visa sponsorship jobs in Georgia are concentrated in the Atlanta metro and the I-85 corridor, where employers like Pfizer, Novelis, and a growing cluster of clinical research organizations actively hire international talent. Georgia's life sciences sector has expanded significantly, supported by the Georgia Research Alliance and proximity to the CDC and Emory University research ecosystems.
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Get Access To All JobsMake your mark for patients
We are looking for a Senior Principal Programmer (Statistical Computing Environment Business Coordinator) who is collaborative, detail-oriented, and compliance-minded to join our Programming, Visualization and Reporting team, based in Raleigh, NC or Atlanta, GA.
About the role
You will help clinical programming teams move to and work confidently within UCB’s modern Statistical Computing Environment. You will translate clinical reporting needs into well-governed study setups, support compliant platform operations, and help improve the way teams generate, validate, and deliver clinical trial analysis and reporting outputs.
Who you’ll work with
You will work with the Programming, Visualization and Reporting team, statistical programming teams, platform administrators, Biometrics partners, and business stakeholders. You will connect technical and business needs, support users through onboarding and daily operations, and help teams follow consistent, compliant, and practical ways of working.
What you’ll do
You will review and coordinate clinical trial analysis and reporting setup requests, making sure they are complete, accurate, and delivered on time.
You will configure study structures, repositories, datasets, reporting components, and access in line with CDISC and governance requirements.
You will manage role-based access, study configurations, and Git/Azure DevOps resources using approved requests and compliant processes.
You will coordinate environment provisioning with platform administrators so study teams can begin work in a ready and reliable environment.
You will support programming teams during onboarding, transition from legacy systems, and ongoing operations as a first-line technical contact.
You will improve lifecycle management and workflows by documenting processes, supporting validation activities, and automating practical solutions that enhance quality and user experience.
Interested? For this position you’ll need the following education, experience and skills:
You bring 5+ years of experience in clinical trial results generation, reporting, and submission processes.
You have experience supporting Statistical Computing Environments, including process flows, user access, and Biometrics requirements.
You understand CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and Listings.
You have worked in regulated pharmaceutical environments and understand SDLC, validation, audit readiness, and compliant configuration expectations.
You can communicate clearly with technical teams and business stakeholders, while tracking setup processes across systems and teams.
You bring practical experience with tools such as Domino Data Lab, SAS, R, Git, Azure DevOps, VS Code, or SAS Studio.
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9,000 people in all four corners of the globe, inspired by patients and driven by science.
Why work with us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.
At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless explicitly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.
UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable federal, state, or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment, your employment with UCB, or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws, orders, and regulations.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
Make your mark for patients
We are looking for a Senior Principal Programmer (Statistical Computing Environment Business Coordinator) who is collaborative, detail-oriented, and compliance-minded to join our Programming, Visualization and Reporting team, based in Raleigh, NC or Atlanta, GA.
About the role
You will help clinical programming teams move to and work confidently within UCB’s modern Statistical Computing Environment. You will translate clinical reporting needs into well-governed study setups, support compliant platform operations, and help improve the way teams generate, validate, and deliver clinical trial analysis and reporting outputs.
Who you’ll work with
You will work with the Programming, Visualization and Reporting team, statistical programming teams, platform administrators, Biometrics partners, and business stakeholders. You will connect technical and business needs, support users through onboarding and daily operations, and help teams follow consistent, compliant, and practical ways of working.
What you’ll do
You will review and coordinate clinical trial analysis and reporting setup requests, making sure they are complete, accurate, and delivered on time.
You will configure study structures, repositories, datasets, reporting components, and access in line with CDISC and governance requirements.
You will manage role-based access, study configurations, and Git/Azure DevOps resources using approved requests and compliant processes.
You will coordinate environment provisioning with platform administrators so study teams can begin work in a ready and reliable environment.
You will support programming teams during onboarding, transition from legacy systems, and ongoing operations as a first-line technical contact.
You will improve lifecycle management and workflows by documenting processes, supporting validation activities, and automating practical solutions that enhance quality and user experience.
Interested? For this position you’ll need the following education, experience and skills:
You bring 5+ years of experience in clinical trial results generation, reporting, and submission processes.
You have experience supporting Statistical Computing Environments, including process flows, user access, and Biometrics requirements.
You understand CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and Listings.
You have worked in regulated pharmaceutical environments and understand SDLC, validation, audit readiness, and compliant configuration expectations.
You can communicate clearly with technical teams and business stakeholders, while tracking setup processes across systems and teams.
You bring practical experience with tools such as Domino Data Lab, SAS, R, Git, Azure DevOps, VS Code, or SAS Studio.
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9,000 people in all four corners of the globe, inspired by patients and driven by science.
Why work with us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.
At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless explicitly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.
UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable federal, state, or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment, your employment with UCB, or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws, orders, and regulations.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
H-1B Biotech & Pharma Job Roles in Georgia
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Search Biotech & Pharma Jobs in GeorgiaBiotech & Pharma H-1B Sponsorship Jobs in Georgia: Frequently Asked Questions
Which biotech & pharma companies sponsor H-1B visas in Georgia?
Georgia-based H-1B visa sponsors in biotech and pharma include large multinationals like Pfizer and Sanofi with Georgia operations, contract research organizations such as ICON and Syneos Health, and biotech firms tied to the Emory and Georgia Tech research ecosystems. The CDC's presence in Atlanta also draws numerous life sciences contractors and research vendors that file H-1B petitions for scientific and technical roles.
Which cities in Georgia have the most biotech & pharma H-1B sponsorship jobs?
Atlanta accounts for the largest share of biotech and pharma H-1B sponsorship activity in Georgia, driven by its concentration of research hospitals, CROs, and pharmaceutical distributors. Athens has a smaller but active cluster linked to the University of Georgia's research programs. Savannah and Augusta have emerging life sciences presences, though Atlanta remains the clear primary market for H-1B candidates in this industry.
What types of biotech & pharma roles typically qualify for H-1B sponsorship in Georgia?
Roles that consistently qualify for H-1B sponsorship in Georgia's biotech and pharma sector include research scientists, bioinformaticians, clinical research associates, regulatory affairs specialists, biostatisticians, and process development engineers. These positions require at least a bachelor's degree in a directly related field such as biology, biochemistry, pharmaceutical sciences, or bioengineering, meeting USCIS's specialty occupation standard. Quality assurance and medical affairs roles with degree-specific requirements also commonly qualify.
How do I find biotech & pharma H-1B sponsorship jobs in Georgia?
Migrate Mate is built specifically for this search, aggregating biotech and pharma positions in Georgia where employers have a documented history of H-1B sponsorship. Rather than filtering through thousands of general job listings, Migrate Mate surfaces roles from companies that have filed H-1B petitions, so you can focus your applications on Georgia employers who are already familiar with the sponsorship process for life sciences candidates.
Are there any Georgia-specific considerations for H-1B sponsorship in biotech & pharma?
Georgia does not have state-level visa sponsorship requirements, so the federal H-1B process applies uniformly. However, Georgia's life sciences hiring is closely tied to federally funded research institutions like the CDC and Emory, where grant-dependent positions can affect sponsorship timelines if funding cycles shift. Candidates should also be aware that many Georgia CROs staff project-based roles, which can raise questions about employer-employee relationships during USCIS adjudication.
What is the prevailing wage for H-1B biotech & pharma jobs in Georgia?
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.