Alkermes Visa Sponsorship Jobs USA
Alkermes is a biopharmaceutical company focused on central nervous system disorders and addiction treatment, with a genuine track record of sponsoring international talent across multiple visa categories. For skilled professionals in drug development, clinical research, and regulatory affairs, Alkermes is a legitimate sponsorship option worth pursuing.
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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.
Job Roles at Alkermes
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Get Access To All JobsTips for Finding Alkermes Visa Sponsorship Jobs USA
Target roles in drug development and clinical science
Alkermes's core work in CNS and addiction therapeutics drives demand for scientists, clinical researchers, and pharmacologists. These specialized roles are strong candidates for visa sponsorship, so focus your applications on positions aligned with the company's therapeutic pipeline.
Understand which visa types Alkermes actually files
Alkermes sponsors H-1B, E-3, TN, and Green Card pathways, along with F-1 OPT and CPT. Knowing this upfront helps you frame your eligibility correctly in outreach and interviews rather than discovering mid-process that your visa type isn't supported.
Australian candidates should highlight E-3 eligibility early
Alkermes has sponsored E-3 visas, making it a genuine option for Australian professionals. Mentioning your E-3 eligibility early in conversations removes a common employer hesitation and signals that sponsorship for you carries lower cost and complexity than H-1B.
Align your application to Alkermes's regulatory and manufacturing functions
Beyond the lab, roles in regulatory affairs, quality assurance, and pharmaceutical manufacturing at Alkermes have historically attracted sponsored hires. If your background spans these areas, position your skills against their commercial-stage pipeline needs.
Use a platform that filters by verified sponsorship history
Not every Alkermes job listing will flag visa sponsorship explicitly. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history and prioritize roles where international candidates have actually been hired before.
Engage Alkermes's talent acquisition team with sponsorship context ready
Alkermes has an active sponsorship track record, so recruiters are familiar with the process. Come prepared with your visa status, timeline, and work authorization details so conversations move efficiently rather than stalling at the sponsorship question.
Frequently Asked Questions
Does Alkermes sponsor H-1B visas?
Yes, Alkermes sponsors H-1B visas and has a consistent track record of doing so across its scientific and technical workforce. Roles in clinical development, pharmacology, data science, and regulatory affairs are among those most likely to receive H-1B sponsorship. If you're targeting Alkermes on an H-1B, prioritizing roles tied to their core CNS and addiction treatment pipeline gives you the strongest positioning.
Which visa types does Alkermes sponsor?
Alkermes sponsors a range of visa categories including H-1B, E-3 visa, TN visa, F-1 OPT, F-1 CPT, and Green Card pathways such as EB-2 and EB-3. This breadth makes Alkermes accessible to international candidates from multiple countries and at different stages of their immigration journey, from students on OPT to professionals seeking permanent residence.
Which departments or roles at Alkermes are most likely to offer visa sponsorship?
Sponsorship at Alkermes tends to concentrate in roles requiring specialized scientific or technical expertise. Clinical research, drug development, pharmacokinetics, regulatory affairs, and quality assurance are areas where the company has historically brought in sponsored talent. Corporate and administrative roles are less commonly sponsored, so candidates with life sciences or pharmaceutical backgrounds have the clearest path.
How do I find open roles at Alkermes that offer visa sponsorship?
The most reliable approach is to use Migrate Mate, which tracks verified sponsorship histories so you can identify Alkermes positions where international candidates have genuinely been sponsored. Alkermes does not always flag sponsorship explicitly in job postings, so filtering through a platform that surfaces real filing data saves significant time and guesswork in your job search.
How do I approach the Alkermes application process as an international candidate?
Disclose your visa status early and frame it as straightforward rather than a complication. Alkermes's talent acquisition team has handled sponsorship across multiple visa categories, so they're not unfamiliar with the process. Have your current status, authorized work period, and any upcoming deadlines ready to share. Applying to roles that closely match Alkermes's therapeutic focus areas will put you in the strongest position for a sponsorship conversation.