Biogen Visa Sponsorship Jobs USA
Biogen is a global biotechnology company and a consistent visa sponsor in the life sciences sector. Known for its work in neuroscience, rare diseases, and biosimilars, Biogen actively sponsors H-1B visa, Green Card, F-1 OPT, TN visa, and J-1 visas, making it a strong option for international professionals in research, clinical development, and regulatory roles.
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Get Access To All JobsPosition Job Title: Senior Principal Risk Based Quality Management Data Monitor
Location: Research Triangle Park, NC (preferred, not mandatory)
About This Role
As a Senior Principal Risk Based Quality Management Data Monitor, you will be a key contributor to the creation of Biogen’s in-house RBQM strategy and process implementation. You will play a critical role in shaping how clinical trial data is monitored, protected, and elevated to the highest quality standards. You will be at the forefront of implementing Risk-Based Quality Management (RBQM) strategies—ensuring patient safety, regulatory compliance, and data integrity across all phases of clinical research. You’ll collaborate closely with biostatistics, data science, safety/pharmacovigilance, clinical operations, and vendors to detect and triage signals early, optimize KRIs/QTLs, and drive continuous process and technology improvements across the portfolio.
This position is ideal for someone who thrives on analytical thinking, cross-functional collaboration, and using RBQM and advanced analytics to keep clinical trials running smoothly and safely.
What You’ll Do
- Risk Identification & Assessment
- Partner with cross functional teams to identify critical data and processes (CDPs) and associated study risks
- Contribute significantly to the development and maintenance of the study-specific Risk Assessment Categorization Tool (RACT) or equivalent by providing a clinical data management focused perspective
- Prioritize risks and signals based on patient safety impact, data integrity, severity, likelihood, and detectability
- Centralized Monitoring
- Conduct proactive, ongoing data reviews using RBQM dashboards and analytics tools
- Ensure timely escalation and follow up on any signals or anomalies
- Triaging: Prioritize, Escalate, and Track signals
- Data Quality Oversight
- Review and validate data across EDC, safety, and other clinical systems to ensure consistency and quality
- Oversee data cleaning timelines and ensure adherence to risk mitigation plans
- Partner with study teams to ensure data flow mapping supports early risk detection
- Issue Management
- Document and communicate findings clearly and effectively to study teams
- Trigger and/or support Corrective and Preventive Actions (CAPA)
- Participate in root cause analyses for major deviations or quality concerns
- Compliance & Governance
- Ensure alignment with ICH-GCP, FDA/EMA regulations, and internal SOPs.
- Support audit and inspection readiness related to RBQM and centralized monitoring
- Technology Enablement & Continuous Improvement
- Contribute to and/or lead process enhancements, technology upgrades, and RBQM best practices
- Partner with platform/analytics teams to enhance dashboards and detection logic; perform UAT and help shape product roadmaps
- Provide training, guidance, and mentorship on RBQM concepts to study teams.
Who You Are
You’re a data-driven problem solver with a deep understanding of clinical trial operations. You excel in fast-paced, matrixed environments and are energized by collaborating with diverse teams. You can spot data issues before they escalate. You anticipate risk, communicate insights clearly, drive actions, and continuously look for ways to improve processes. You balance rigor with pragmatism, communicate crisply across functions, and stay laser focused on patient safety and data integrity.
Required Skills
- 7+ years of experience in clinical data management, clinical operations or Academia with strong scientific knowledge in at least one therapeutic area within the Biogen portfolio
- RBQM-focused roles within pharma or CRO settings
- Hands-on experience with centralized monitoring tools (RBQM platforms/dashboards), KRIs, QTLs, or similar RBQM methodologies
- Proficiency with EDC systems and data visualization tools
- High attention to detail including proven ability to manage multiple, competing priorities
- Experience supporting audits/inspections
- Understanding of clinical data flow, study endpoints, and regulatory requirements
- Strong analytical and critical-thinking abilities
- Excellent communication and stakeholder management skills
- Ability to adapt and thrive in a dynamic, cross-functional environment
- Risk-based thinking & structured problem-solving
- Data driven decision-making
- Collaborative teamwork across clinical and operational functions
- Deep understanding of drug development and biopharmaceutical industry required
- Fluent English (oral and written)
- Demonstrated ability to identify data trends, signals, outliers, and risk indicators using listings, visualizations, metrics, and analytics tools
- Strong knowledge of GCP, ICH E6(R2)/E6(R3), regulatory expectations, and industry data quality best practices
- Demonstrated problem-solving skills with a continuous improvement mindset and enthusiasm for scientific data excellence.
Education Requirements/Preferred Skills
- Bachelor’s degree in life sciences, health sciences, pharmacy, nursing, data science, or related discipline; advanced degree (MS, PharmD, PhD) strongly preferred
- Experience with implementing consistent clinical and scientific data review processes
- Experience defining and calibrating KRIs/QTLs at study and portfolio levels
- Experience with cross study trending and systemic risk analysis
- Therapeutic area familiarity aligned to portfolio (e.g., neuroscience, rare disease, immunology)
Why Biogen?
Our mission to find therapies for neurological and rare diseases is a unique focus within our industry, and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients’ lives and on changing the course of medicine. Together, we pioneer. Together, we thrive.
Job Level: Management
Additional Information
The base compensation range for this role is: -
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being; including, but not limited to:
- Medical, Dental, Vision, & Life insurances
- Fitness & Wellness programs including a fitness reimbursement
- Short- and Long-Term Disability insurance
- A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
- Up to 12 company paid holidays + 3 paid days off for Personal Significance
- 80 hours of sick time per calendar year
- Paid Maternity and Parental Leave benefit
- 401(k) program participation with company matched contributions
- Employee stock purchase plan
- Tuition reimbursement of up to $10,000 per calendar year
- Employee Resource Groups participation
Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our Biogen.
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.
Position Job Title: Senior Principal Risk Based Quality Management Data Monitor
Location: Research Triangle Park, NC (preferred, not mandatory)
About This Role
As a Senior Principal Risk Based Quality Management Data Monitor, you will be a key contributor to the creation of Biogen’s in-house RBQM strategy and process implementation. You will play a critical role in shaping how clinical trial data is monitored, protected, and elevated to the highest quality standards. You will be at the forefront of implementing Risk-Based Quality Management (RBQM) strategies—ensuring patient safety, regulatory compliance, and data integrity across all phases of clinical research. You’ll collaborate closely with biostatistics, data science, safety/pharmacovigilance, clinical operations, and vendors to detect and triage signals early, optimize KRIs/QTLs, and drive continuous process and technology improvements across the portfolio.
This position is ideal for someone who thrives on analytical thinking, cross-functional collaboration, and using RBQM and advanced analytics to keep clinical trials running smoothly and safely.
What You’ll Do
- Risk Identification & Assessment
- Partner with cross functional teams to identify critical data and processes (CDPs) and associated study risks
- Contribute significantly to the development and maintenance of the study-specific Risk Assessment Categorization Tool (RACT) or equivalent by providing a clinical data management focused perspective
- Prioritize risks and signals based on patient safety impact, data integrity, severity, likelihood, and detectability
- Centralized Monitoring
- Conduct proactive, ongoing data reviews using RBQM dashboards and analytics tools
- Ensure timely escalation and follow up on any signals or anomalies
- Triaging: Prioritize, Escalate, and Track signals
- Data Quality Oversight
- Review and validate data across EDC, safety, and other clinical systems to ensure consistency and quality
- Oversee data cleaning timelines and ensure adherence to risk mitigation plans
- Partner with study teams to ensure data flow mapping supports early risk detection
- Issue Management
- Document and communicate findings clearly and effectively to study teams
- Trigger and/or support Corrective and Preventive Actions (CAPA)
- Participate in root cause analyses for major deviations or quality concerns
- Compliance & Governance
- Ensure alignment with ICH-GCP, FDA/EMA regulations, and internal SOPs.
- Support audit and inspection readiness related to RBQM and centralized monitoring
- Technology Enablement & Continuous Improvement
- Contribute to and/or lead process enhancements, technology upgrades, and RBQM best practices
- Partner with platform/analytics teams to enhance dashboards and detection logic; perform UAT and help shape product roadmaps
- Provide training, guidance, and mentorship on RBQM concepts to study teams.
Who You Are
You’re a data-driven problem solver with a deep understanding of clinical trial operations. You excel in fast-paced, matrixed environments and are energized by collaborating with diverse teams. You can spot data issues before they escalate. You anticipate risk, communicate insights clearly, drive actions, and continuously look for ways to improve processes. You balance rigor with pragmatism, communicate crisply across functions, and stay laser focused on patient safety and data integrity.
Required Skills
- 7+ years of experience in clinical data management, clinical operations or Academia with strong scientific knowledge in at least one therapeutic area within the Biogen portfolio
- RBQM-focused roles within pharma or CRO settings
- Hands-on experience with centralized monitoring tools (RBQM platforms/dashboards), KRIs, QTLs, or similar RBQM methodologies
- Proficiency with EDC systems and data visualization tools
- High attention to detail including proven ability to manage multiple, competing priorities
- Experience supporting audits/inspections
- Understanding of clinical data flow, study endpoints, and regulatory requirements
- Strong analytical and critical-thinking abilities
- Excellent communication and stakeholder management skills
- Ability to adapt and thrive in a dynamic, cross-functional environment
- Risk-based thinking & structured problem-solving
- Data driven decision-making
- Collaborative teamwork across clinical and operational functions
- Deep understanding of drug development and biopharmaceutical industry required
- Fluent English (oral and written)
- Demonstrated ability to identify data trends, signals, outliers, and risk indicators using listings, visualizations, metrics, and analytics tools
- Strong knowledge of GCP, ICH E6(R2)/E6(R3), regulatory expectations, and industry data quality best practices
- Demonstrated problem-solving skills with a continuous improvement mindset and enthusiasm for scientific data excellence.
Education Requirements/Preferred Skills
- Bachelor’s degree in life sciences, health sciences, pharmacy, nursing, data science, or related discipline; advanced degree (MS, PharmD, PhD) strongly preferred
- Experience with implementing consistent clinical and scientific data review processes
- Experience defining and calibrating KRIs/QTLs at study and portfolio levels
- Experience with cross study trending and systemic risk analysis
- Therapeutic area familiarity aligned to portfolio (e.g., neuroscience, rare disease, immunology)
Why Biogen?
Our mission to find therapies for neurological and rare diseases is a unique focus within our industry, and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients’ lives and on changing the course of medicine. Together, we pioneer. Together, we thrive.
Job Level: Management
Additional Information
The base compensation range for this role is: -
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being; including, but not limited to:
- Medical, Dental, Vision, & Life insurances
- Fitness & Wellness programs including a fitness reimbursement
- Short- and Long-Term Disability insurance
- A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
- Up to 12 company paid holidays + 3 paid days off for Personal Significance
- 80 hours of sick time per calendar year
- Paid Maternity and Parental Leave benefit
- 401(k) program participation with company matched contributions
- Employee stock purchase plan
- Tuition reimbursement of up to $10,000 per calendar year
- Employee Resource Groups participation
Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our Biogen.
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.
Job Roles at Biogen
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Get Access To All JobsTips for Finding Biogen Visa Sponsorship Jobs USA
Target roles in research and clinical development
Biogen's sponsorship activity is concentrated in scientific and technical functions. Roles in neuroscience research, clinical operations, biostatistics, and regulatory affairs align closely with the specialty occupation criteria that H-1B and EB-2 petitions require.
Use your F-1 OPT as a foot in the door
Biogen sponsors F-1 OPT and CPT, making it accessible for students currently completing life sciences or engineering degrees. A stint on OPT often precedes H-1B sponsorship, so treat it as a long-term sponsorship pathway rather than a temporary arrangement.
Understand Biogen's Green Card track record
Biogen sponsors both EB-2 and EB-3 Green Cards, which signals long-term investment in international hires. When negotiating or evaluating an offer, it's reasonable to ask about the company's typical timeline from H-1B to permanent residency sponsorship.
Canadian and Mexican professionals should explore the TN visa
Biogen sponsors TN visas, which don't require lottery selection and can be processed quickly. If you hold a qualifying degree in a USMCA-listed occupation such as scientist, pharmacist, or engineer, the TN may get you working at Biogen faster than the H-1B route.
Search for open roles before the H-1B registration window
Biogen needs to register H-1B candidates in March for an October start date. Targeting Biogen roles in the preceding months gives both sides time to assess fit. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history and apply with confidence.
Highlight domain-specific expertise in your application
Biogen's hiring in Healthcare and Medical Services is highly specialized. Candidates with direct experience in neurodegenerative diseases, rare disease drug development, or biosimilar manufacturing stand out because these areas reflect Biogen's core therapeutic focus and are harder to fill domestically.
Frequently Asked Questions
Does Biogen sponsor H-1B visas?
Yes, Biogen sponsors H-1B visas and has a strong track record of doing so across its U.S. operations. Sponsorship is most common in scientific, clinical, regulatory, and engineering roles that meet the specialty occupation standard. If you're targeting Biogen, roles requiring a specific degree in a technical or life sciences field are your strongest candidates for H-1B sponsorship.
Which visa types does Biogen sponsor?
Biogen sponsors a broad range of visa types including H-1B, EB-2, EB-3 Green Cards, F-1 OPT, F-1 CPT, TN visa, and J-1. This range reflects a company that hires internationally across multiple stages of a career, from students on OPT to senior professionals seeking permanent residence.
Which departments or roles at Biogen are most likely to receive visa sponsorship?
Sponsorship at Biogen is concentrated in roles tied to its core business in neuroscience, rare diseases, and biosimilars. Research scientists, clinical data managers, biostatisticians, regulatory affairs specialists, and manufacturing engineers are among the functions most associated with sponsored positions. Corporate and generalist roles are less frequently sponsored.
How do I find visa-sponsored job openings at Biogen?
Migrate Mate is the most efficient way to find roles at Biogen that come with real sponsorship history attached. You can filter specifically for Biogen and the visa type you need, rather than applying blindly and hoping sponsorship comes up during the process. This saves time and targets your effort where it counts.
How do I approach the application timeline if I need H-1B sponsorship at Biogen?
The H-1B cap registration window opens in March each year, with an October 1 start date for selected candidates. Biogen needs enough lead time to evaluate your fit, prepare the petition, and register before the deadline. Aiming to have an offer in place by January or February gives both parties the best chance of meeting that window without rushing.