Alkermes H-1B Visa Sponsorship Jobs USA
Alkermes sponsors H-1B visas for specialized roles across its drug development and commercial operations, particularly in scientific, clinical, and technical disciplines. The company has a consistent sponsorship track record in the biotechnology and pharmaceuticals sector, making it a viable target for international candidates with relevant qualifications.
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An exciting opportunity to lead the strategic and operational management of complex clinical supply activities across all phases of development to provide life-changing therapeutics for patients. The Senior Director of Clinical Supply Chain ensures the uninterrupted, compliant, and cost-effective delivery of investigational products to global clinical trial sites. The ideal candidate will bring deep expertise in supply chain strategy, vendor oversight, and cross-functional collaboration, with a strong understanding of GMP, IRT systems, and regulatory requirements.
Responsibilities
Strategic Leadership
- Develop and execute global clinical supply chain strategies aligned with corporate and clinical development goals.
- Lead long-range planning and drive the continued development and transformation of supply chain infrastructure to meet the needs of the growing business.
- Partner with Legal, Finance, Trade Compliance, Quality Assurance, Regulatory Affairs, Clinical Operations, CMC Teams, and other functions across the internal network, to deliver responsibilities aligned with business goals.
Operational Oversight
- Oversee demand forecasting, inventory management, and supply planning using simulation tools.
- Manage packaging, labeling, distribution, and returns of clinical trial materials (CTM) in compliance with GMP and global regulations.
- Lead IRT system design, implementation, and user acceptance testing for effective drug tracking and randomization.
Vendor and Budget Management
- Lead senior level business relationship management with CMOs and third-party logistics providers; develop and ensure adherence to contracts and KPIs.
- Collaborate with Quality Assurance leadership on vendor qualification and audits.
- Develop and manage clinical supply budgets, ensuring cost-effective operations.
- Partner with program project managers to align clinical supply budgets with overall program financial planning and ensure transparency in forecasting, tracking, and reporting.
Compliance and Inspection Readiness
- Ensure inspection readiness for global regulatory audits.
- Maintain documentation and SOPs to support compliance and continuous improvement.
Team Leadership
- Mentor and continue to build a high-performing clinical supply chain team.
- Foster a culture of accountability, innovation, and cross-functional collaboration.
Qualifications
QUALIFICATIONS
- Bachelor’s degree in Life Sciences, Pharmacy, Supply Chain, or related field (advanced degree preferred).
- 15+ years of experience in clinical supply chain management within the pharmaceutical or biotech industry.
- Proven leadership in global clinical supply operations, including late-stage and commercial transition.
- Strong knowledge of GMP, IRT systems, and regulatory requirements.
- Excellent communication, project management, and vendor negotiation skills.
Alkermes has recently adopted a hybrid working environment to support and meet the needs of employees and this role will operate in a flexible environment with 60% of time in the office and 40% from home. This position is eligible for the hybrid workplace model, requiring work to be completed onsite at our Waltham, MA office at least 3 days per week. This role is not eligible for fully remote.
The annual base salary for this position ranges from $255,000 to $270,000. In addition, this position is eligible for an annual performance pay bonus. Exact compensation may vary based on skills, training, knowledge, and experience. Alkermes offers a competitive benefits package.
About us
Why join Team Alkermes?
Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders. We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts’ Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine.
Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer.
Job Description
An exciting opportunity to lead the strategic and operational management of complex clinical supply activities across all phases of development to provide life-changing therapeutics for patients. The Senior Director of Clinical Supply Chain ensures the uninterrupted, compliant, and cost-effective delivery of investigational products to global clinical trial sites. The ideal candidate will bring deep expertise in supply chain strategy, vendor oversight, and cross-functional collaboration, with a strong understanding of GMP, IRT systems, and regulatory requirements.
Responsibilities
Strategic Leadership
- Develop and execute global clinical supply chain strategies aligned with corporate and clinical development goals.
- Lead long-range planning and drive the continued development and transformation of supply chain infrastructure to meet the needs of the growing business.
- Partner with Legal, Finance, Trade Compliance, Quality Assurance, Regulatory Affairs, Clinical Operations, CMC Teams, and other functions across the internal network, to deliver responsibilities aligned with business goals.
Operational Oversight
- Oversee demand forecasting, inventory management, and supply planning using simulation tools.
- Manage packaging, labeling, distribution, and returns of clinical trial materials (CTM) in compliance with GMP and global regulations.
- Lead IRT system design, implementation, and user acceptance testing for effective drug tracking and randomization.
Vendor and Budget Management
- Lead senior level business relationship management with CMOs and third-party logistics providers; develop and ensure adherence to contracts and KPIs.
- Collaborate with Quality Assurance leadership on vendor qualification and audits.
- Develop and manage clinical supply budgets, ensuring cost-effective operations.
- Partner with program project managers to align clinical supply budgets with overall program financial planning and ensure transparency in forecasting, tracking, and reporting.
Compliance and Inspection Readiness
- Ensure inspection readiness for global regulatory audits.
- Maintain documentation and SOPs to support compliance and continuous improvement.
Team Leadership
- Mentor and continue to build a high-performing clinical supply chain team.
- Foster a culture of accountability, innovation, and cross-functional collaboration.
Qualifications
QUALIFICATIONS
- Bachelor’s degree in Life Sciences, Pharmacy, Supply Chain, or related field (advanced degree preferred).
- 15+ years of experience in clinical supply chain management within the pharmaceutical or biotech industry.
- Proven leadership in global clinical supply operations, including late-stage and commercial transition.
- Strong knowledge of GMP, IRT systems, and regulatory requirements.
- Excellent communication, project management, and vendor negotiation skills.
Alkermes has recently adopted a hybrid working environment to support and meet the needs of employees and this role will operate in a flexible environment with 60% of time in the office and 40% from home. This position is eligible for the hybrid workplace model, requiring work to be completed onsite at our Waltham, MA office at least 3 days per week. This role is not eligible for fully remote.
The annual base salary for this position ranges from $255,000 to $270,000. In addition, this position is eligible for an annual performance pay bonus. Exact compensation may vary based on skills, training, knowledge, and experience. Alkermes offers a competitive benefits package.
About us
Why join Team Alkermes?
Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders. We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts’ Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine.
Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer.
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Get Access To All JobsTips for Finding Alkermes H-1B Jobs
Target roles aligned with your scientific or technical background
Alkermes prioritizes H-1B sponsorship for positions requiring specialized expertise, particularly in drug development, clinical research, regulatory affairs, and biostatistics. Focus your applications on roles where your degree and experience map directly to the job requirements.
Engage with Alkermes's neuroscience and addiction treatment focus
Alkermes concentrates its pipeline on neuroscience and addiction medicine. Candidates who can speak to relevant therapeutic area knowledge during interviews signal immediate value, which strengthens the business case an employer needs to justify H-1B sponsorship.
Confirm sponsorship willingness early in the process
Pharmaceutical companies vary by role and hiring manager on sponsorship decisions. Raise visa status professionally during the recruiter screening call rather than waiting until an offer is made, so both sides avoid wasted time.
Use verified sponsorship data when searching for open roles
Not every job listing makes sponsorship clear. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history, helping you identify active Alkermes openings where international candidates are genuinely considered.
Understand the H-1B cap and Alkermes's filing timeline
H-1B cap registrations open in March for an October 1 start date. If you need cap-subject sponsorship, align your Alkermes job search and interview process to ensure an offer is in place well before the registration window opens.
Highlight cross-functional experience relevant to biopharma operations
Alkermes runs integrated manufacturing, clinical, and commercial functions. Candidates with experience spanning multiple biopharma disciplines, such as CMC, quality assurance, or medical affairs, are more likely to be considered for H-1B sponsorship given their broader organizational value.
Alkermes H-1B Visa Sponsorship: Frequently Asked Questions
Does Alkermes sponsor H-1B visas?
Yes, Alkermes sponsors H-1B visas for qualifying roles. The company operates in biotechnology and pharmaceuticals, where specialized scientific and technical talent is often sourced internationally. Sponsorship is most consistently offered for positions requiring advanced degrees or niche expertise in areas like drug development, clinical research, and regulatory science.
Which departments at Alkermes are most likely to offer H-1B sponsorship?
H-1B sponsorship at Alkermes tends to concentrate in roles requiring specialized qualifications. Research and development, clinical operations, biostatistics, regulatory affairs, medical affairs, and manufacturing science positions are strong candidates. Corporate functions such as finance or general administration are less commonly associated with H-1B filings at pharmaceutical companies of this size.
How do I navigate the H-1B application process at Alkermes?
Once Alkermes extends an offer to a sponsored candidate, their legal team or an external immigration firm files the Labor Condition Application with the Department of Labor, followed by the H-1B petition with USCIS. As the candidate, your primary responsibility is providing accurate documentation. The employer manages the filing process and associated costs under federal rules.
How do I find H-1B jobs at Alkermes that are open to international candidates?
Alkermes posts openings on its careers page, but listings rarely specify visa sponsorship availability. Migrate Mate aggregates roles from verified H-1B sponsors and lets you filter specifically for companies with a sponsorship history, which helps you identify Alkermes positions where international applications are genuinely welcomed rather than screening them out.
How long does the H-1B sponsorship process take at Alkermes?
Timeline depends on where you are in the H-1B cycle. Cap-subject petitions require lottery selection in March and have an October 1 start date, meaning the process spans six or more months from registration to work authorization. If you are already in H-1B status with another employer, an Alkermes transfer can often be filed with a quicker turnaround using premium processing.
What is the prevailing wage for H-1B jobs at Alkermes?
H-1B employers must pay at least the prevailing wage, which is determined when they file the Labor Condition Application with the Department of Labor. The rate is based on the role, location, and experience level, and ensures international hires are paid comparably to U.S. workers in the same position. You can look up prevailing wage rates for any occupation and location using the DOL's OFLC Wage Search tool.