AstraZeneca Posted November 3, 2026

Senior Manager, Cell Therapy Hub

Wilmington, Delaware, United States of America Full time
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AstraZeneca is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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

Nurse Coordinator

Apheresis Nurse

Cell Laboratory Professional

Quality Manager

Other patient-focused cell therapy or oncology operational roles

Experience managing complex patient journeys and coordinating across multiple cross-functions

Ability to solve site-facing operational challenges and effectively navigate organizational complexity.

Strong communication, collaboration, and relationship-building skills.

Experience working across multiple digital platforms and systems.

Strong organizational and project management capabilities with exceptional attention to detail.

Ability to work independently in a fast-paced, patient-focused environment.

Desirable Skills/Experience

Advanced degree in Life Sciences, Healthcare, Engineering, or a related field (e.g., PharmD, Nurse Practitioner, Physician Assistant, Biomedical Engineering).

Experience supporting cell and gene therapy programs.

Experience working with critical raw material suppliers and/or contract manufacturing organizations (CMOs).

Knowledge of oncology, immuno-oncology, and cellular therapy treatment pathways.

Familiarity with GMP, GCP, and regulated healthcare environments.

Experience developing SOPs, training programs, and process improvement initiatives.

Why AstraZeneca

Here, courage, curiosity, and collaboration fuel a relentless focus on transforming cancer outcomes, powered by a pipeline that fuses innovative science with advanced technology. You will work in an environment where unexpected teams come together to spark bold ideas, backed by meaningful investment and a clear path from discovery to impact. We value kindness alongside ambition, and we empower leaders at every level to ask sharp questions, take smart risks, and turn data into decisions that help patients sooner.

Compensation & Benefits

The annual base pay for this position ranges from $137,937.60 - $206,906.40. Our positions offer eligibility for various incentives, an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility.

Join us in our unique and ambitious world.

Date Posted

03-Nov-2026

Closing Date

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

Job details

Seniority
Manager
Function
Clinical Development
Therapeutic area
Not listed
Location
Wilmington, Delaware, United States of America
Employment type
Full time

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 433 comparable Manager Clinical Development roles across 67 biopharma companies.

433Comparable roles tracked
394Currently active
67Companies hiring similar roles
39Countries represented

Salary context

135 of 433 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Site Contracts Associate, IQVIA Biotech · IQVIA $49,200/yr – $123,000/yr
Highest disclosed · Associate Director, Clinical Development · Gilead Sciences, Inc. $210,375/yr – $272,250/yr
Peer group range $86,100 – $241,313 (median $180,500)

Where these roles are based

Top locations among the 433 comparable roles

United States197
India55
United Kingdom24
China20
Japan14
Poland14

+ 33 more countries

Seniority mix

433 of 433 peers have a known seniority level

Manager270
Associate Director118
Associate45

Therapeutic area mix

36 of 433 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology19
Immunology7
Dermatology & Aesthetics2
Neuroscience2
Ophthalmology2
Cardiovascular / CVRM2
Respiratory2

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
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Notify me about similar jobs

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.