Skills this job asks for
Construction managementSupply chainLogisticsPatient careCompliance
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Sponsorship verdict
Sponsorship possible
One solid signal, not two. Worth applying, and worth asking about sponsorship early.
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✓
Employer is on a government sponsor recordThe US Department of Labor certified 99 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first.
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The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
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No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area.
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✓
What Astrazeneca Pharmaceuticals Lp paid sponsored hires in similar roles12 certified filings for “Assoc.
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Confirmed live todayWhen a source last listed this job as open.
Details and sources
- Employer is on a government sponsor record
- The US Department of Labor certified 99 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. Source: LCA disclosure data (US Department of Labor (OFLC)).
- No salary bar for this route
- H-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
- What Astrazeneca Pharmaceuticals Lp paid sponsored hires in similar roles
- 12 certified filings for “Assoc. Princ. Scientist, Vector Engineering & Cell Line Dev.” (Molecular and Cellular Biologists) in MD: $103k–$158k, median $136k. Most were filed at wage level IV (33%) — 4 lottery entries, ≈61% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
A verdict summarises public evidence. It is not legal advice and never a guarantee: the employer and the immigration authority decide. Sign in to factor in where you can already work.
About the role
At AstraZeneca, we follow the science to explore and innovate, working to treat, prevent, modify, and ultimately cure some of the world's most complex diseases. Within our Cell Therapy organization, we are advancing cutting-edge science and technology to transform outcomes for patients with cancer.
We are seeking a Senior Manager, Cell Therapy Hub to join our Cell Therapy Patient Operations team supporting clinical and commercial cell therapy production across multiple sites. This field-based role serves as a critical connection point between treatment centers, healthcare professionals, patients, and AstraZeneca cross-functional teams, ensuring a seamless vein-to-vein (V2V) patient journey.
The successful candidate will demonstrate expertise in patient coordination, provider support, and cell therapy operations while delivering an exceptional experience for treatment sites and patients. Reporting to the Senior Director, Cell Therapy Hub, this position plays a key role in advancing life-changing cell therapy treatments through operational excellence and patient-centered support.
As the Senior Manager, Cell Therapy Hub, you will:
• Serve as a trusted, knowledgeable single point of contact for treatment site collaborators, improving the site experience through the AstraZeneca Cell Therapy Hub.
• Independently manage all patient vein-to-vein workflows from patient registration through infusion within assigned geographic regions.
• Identify, raise, and resolve patient-related issues while providing coverage support across regions as needed.
• Partner closely with cross-functional teams including Clinical Operations, Site Management, Supply Chain, Medical Affairs, Information Technology, Commercial, and other team members to meet patient and healthcare provider needs.
• Communicate critical patient-related information to site collaborators with empathy and professionalism while managing expectations.
• Collaborate with Regional and Territory Operations Managers to ensure site logistics, personnel readiness, and Chain of Identity (COI)/Chain of Custody (COC) access to AstraZeneca digital platforms.
• Coordinate communication and resolution of issues related to cellular starting materials, investigational medicinal products (IMPs), and associated supplies.
• Partner with Quality Assurance, Manufacturing, and Supply Chain teams on out-of-specification (OOS) communications, product recalls, and product-related site issues.
• Develop and maintain internal and external standard operating procedures (SOPs), training materials, and operational documentation related to the Cell Therapy Hub.
• Demonstrate proficiency in all Cell Therapy Hub systems, including Customer Portal and telephony platforms, as well as associated SOPs, work instructions, and business processes.
• Drive continuous improvement initiatives and contribute to the development of innovative solutions that enhance the patient care experience.
• Maintain compliance with AstraZeneca policies, regulatory standards, and Cell Therapy Hub procedures.
• Support implementation and rollout of process improvements and operational changes across assigned treatment sites.
• Demonstrate a strong commitment to patients by consistently reflecting AstraZeneca values in daily interactions and decision-making.
• Perform other duties as assigned while maintaining adherence to applicable regulations and SOPs.
• Travel greater than 50% as required.
Essential Skills/Experience
• Bachelor's degree in Life Sciences, Healthcare, Nursing, Business, or a related field, or equivalent combination of education and experience.
• Minimum of 4 years of experience within a cell therapy program, healthcare system, or regulated healthcare environment in roles such as:
• Research Coordinator
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