Alkermes E-3 Visa Sponsorship Jobs USA
Alkermes sponsors E-3 visas for Australian professionals in biotechnology and pharmaceuticals, with roles typically spanning drug development, clinical research, regulatory affairs, and scientific operations. The company has an established sponsorship infrastructure across its U.S. sites, making it a credible target for Australian specialists in life sciences.
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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 E-3 Visa Sponsorship Jobs USA
Align your degree to specialty occupation criteria
Alkermes files E-3 petitions for roles requiring a directly related bachelor's degree or higher. Map your Australian qualification to the specific job title using O*NET to confirm your field satisfies the specialty occupation requirement before applying.
Target roles in clinical and regulatory functions
Alkermes's E-3 filings cluster around scientific and clinical functions rather than general business roles. Focus your search on clinical operations, regulatory affairs, pharmacovigilance, and laboratory science positions at their U.S. facilities.
Verify your degree equivalency before interviews
Australian three-year bachelor's degrees are generally accepted as equivalent to U.S. four-year degrees for E-3 purposes, but Alkermes's HR team may request a credential evaluation from a NACES-approved evaluator to confirm this in writing before filing.
Search verified E-3 sponsors on Migrate Mate
Filter your job search to confirmed E-3 sponsors in biotechnology and pharmaceuticals using Migrate Mate, which surfaces DOL Labor Condition Application data by employer and role so you're targeting companies with real filing history, not just posted intentions.
Ask about the LCA timeline during offer negotiations
Your E-3 can't be approved until Alkermes obtains a certified Labor Condition Application from DOL, which typically takes seven business days. Raise this early so your start date accounts for LCA certification plus consulate appointment scheduling.
Prepare for prevailing wage questions at the offer stage
Alkermes must pay at least the DOL prevailing wage for your role and location. Check the OFLC Wage Search to find the wage level for your occupation and metro area before negotiating, so you know the floor and can identify any discrepancy early.
Alkermes E-3 Visa Sponsorship: Frequently Asked Questions
Does Alkermes sponsor E-3 visas?
Yes, Alkermes sponsors E-3 visas for Australian professionals in roles that meet the specialty occupation requirement. The company operates across biotechnology and pharmaceutical research, development, and clinical functions in the U.S., and has an established process for filing the required Labor Condition Application through DOL and supporting consular applications.
Which roles at Alkermes typically receive E-3 sponsorship?
E-3 sponsorship at Alkermes is most common in scientific and clinical roles, including positions in drug development, clinical operations, regulatory affairs, pharmacovigilance, and laboratory research. These roles require a degree in a directly related field, which aligns with the E-3 specialty occupation definition. General business or administrative roles are less commonly sponsored.
How do I navigate the E-3 application process at Alkermes?
Once you receive an offer, Alkermes's HR or legal team files a Labor Condition Application with DOL for certification. After approval, you complete the DS-160 and attend a consular interview in Australia with the certified LCA, your offer letter, and supporting documents. USCIS is not involved in standard consular E-3 applications. Migrate Mate can manage the filing steps if you want dedicated support.
How long does the E-3 process take at Alkermes?
The DOL LCA certification typically takes around seven business days. After that, consulate appointment availability in Sydney, Melbourne, or Perth determines the overall timeline, which can range from a few weeks to several months depending on demand. Plan for at least four to six weeks from offer acceptance to visa stamp under normal conditions.
How do I strengthen my E-3 application for a role at Alkermes?
Confirm your degree maps to the specific job title using O*NET before applying, and obtain a credential evaluation if your qualification is a three-year Australian degree. During the interview process, request written confirmation of Alkermes's intent to sponsor and the expected LCA filing timeline. Arriving at the consulate with a complete package, including the certified LCA and a detailed offer letter, significantly reduces the risk of additional processing.
What is the prevailing wage for E-3 sponsorship at Alkermes?
E-3 employers must pay at least the prevailing wage, determined when they file a Labor Condition Application with the Department of Labor. The rate is based on the role, location, and experience level, ensuring Australian 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.