A

AstraZeneca

Global pharmaceutical company developing prescription medicines

Delivery Manager

Full-TimeUpdated on 10/1/2026Deadline 10/5/26
$139.9k - $209.9k/yr+ Short-term incentive bonus + Equity-based long-term incentive
Senior
Bachelor's
Gaithersburg, MD, USA
HybridAt least three days per week in the office.

About the job

Requirements
  • Minimum 5 years of experience.
  • Demonstrated experience in program or delivery management, with a proven track record delivering complex, multi-team software initiatives.
  • Demonstrated experience leading multi-functional programs in a technology or digital product organization; experience in highly regulated environments with products deployed in production is preferred.
  • Ability to read and reason about software architecture, APIs, integrations, data flows, environments, and continuous integration/continuous delivery pipelines, and to participate substantively in technical design and planning discussions with senior engineers.
  • Hands-on background in software engineering, DevOps, or a comparable technical team, sufficient to break down technical work, own cross-team technical dependencies, and pressure-test engineering estimates and trade-offs.
  • Ability to lead through ambiguity, create structure where there is none, and drive outcomes without relying on formal authority.
  • Practical, daily experience using AI-assisted tools such as Claude, Copilot, or GPT, and ability to explain how AI has changed the way of working.
  • Experience managing matrixed teams and working globally.
  • Bachelor’s degree required, preferably in a technical or engineering field.
  • Ability to communicate complex technical situations clearly in writing and verbally, and to determine when to escalate issues versus resolve them.
  • Ability to work in person at least three days per week on average.
Responsibilities
  • Break complex, cross-team initiatives into a technically coherent plan of work, understanding architecture, services, integrations, and data flows sufficiently to sequence delivery correctly.
  • Identify, map, and actively manage dependencies across engineering teams, platforms, and external partners, driving them to resolution.
  • Engage in architecture, design, and technical planning discussions; ask informed questions and pressure-test engineering estimates, sequencing, and trade-offs.
  • Anticipate integration, environment, and release risks, including APIs, shared services, data migrations, and continuous integration/continuous delivery constraints, and coordinate technical work to reduce those risks.
  • Translate engineering realities into product and business outcomes so leadership can make informed decisions about technical feasibility and risk.
  • Own delivery of complex, multi-functional initiatives from framing through execution to value realization.
  • Identify dependencies, risks, and blockers early and drive them to resolution.
  • Lead initiative governance by defining appropriate cadences, metrics, and participant groups.
  • Maintain integrated delivery plans grounded in an accurate understanding of the technical work.
  • Manage resources and delivery plans, accountable to the Delivery Director and Head of Delivery Excellence.
  • Ensure product delivery meets quality expectations and complies with Standard Operating Procedures and Policies.
  • Use AI tools such as Claude, GPT, Devin, or Copilot to generate status summaries, analyze delivery and engineering data, draft customer communications, and identify patterns across initiatives.
  • Build and promote AI-assisted delivery practices, including automating routine reporting, surfacing technical risks earlier, and freeing teams to focus on work requiring judgment.
  • Review AI-generated output critically and ensure the accuracy and clarity of communications.
  • Track advances in AI-assisted work management and translate them into practical team-level improvements.
  • Drive continuous planning with Product and Engineering leadership.
  • Maintain a unified portfolio view of progress, direction, and decisions needed from leadership.
  • Use data-driven metrics and performance monitoring to track delivery maturity and align outcomes with product and business value.
  • Track delivery budgets, flag variances, and support informed resourcing decisions.
  • Partner with Product Owners, Engineering Leads, Design Leads, and Customer Implementation Leads to align on completion criteria and hold the organization accountable.
  • Negotiate competing needs of Development and Customer Implementation teams to achieve positive outcomes.
  • Build trusted relationships across engineering and product teams and levels without relying on formal authority.
  • Represent delivery in leadership forums with clarity and perspective.
  • Collaborate with internal and external partners, including global teams.
  • Model a culture of delivery excellence.
  • Lead retrospectives and drive systemic improvements.
  • Help teams distinguish routine activity from factors impeding delivery.
  • Take ownership and hold self and others accountable to outcomes over activity.
Desired Qualifications
  • Experience in digital health, life sciences, or other highly regulated technology environments.
  • Familiarity with GxP, ICH GCP, FDA 21 CFR, GDPR, or similar standards in a delivery context.
  • Global delivery experience across geographies and time zones.
  • Experience building or improving delivery management practices from scratch.
  • Pharmaceutical industry or clinical trial platform experience.
  • Prior experience as a software engineer, technical lead, solutions architect, or in a comparable hands-on technical role.
  • Experience managing delivery financials, including budgets, forecasts, and resourcing models.
  • An advanced degree.

About the company

AstraZeneca develops and markets prescription medicines and vaccines for global health, focusing on oncology, cardiovascular/metabolic, respiratory, and infectious diseases. Its products work by targeting specific biological pathways or cells to treat diseases or prevent infections, using small-molecule drugs, biologics, and vaccines. The company differentiates itself through its dual heritage from Sweden and the UK, a broad pipeline, and strong R&D with collaborations to move from discovery to patient access across multiple therapeutic areas. Its goal is to improve people’s health by discovering, developing, and delivering medicines and vaccines worldwide.

Company Size

10,001+

Company Stage

IPO

Headquarters

Cambridge, United Kingdom

Founded

1913

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Simplify's Take

What believers are saying

  • Sept. 29, 2026 FDA filing for Orpathys-Tagrisso targets EGFR-mutated MET-overexpressing lung cancer.
  • Oct. 2026 Medicare-negotiation appeal keeps AstraZeneca fighting for U.S. pricing power.
  • July 2026 Tagrisso appellate win preserved a blockbuster and validated its patent moat.

What critics are saying

  • Forxiga patents face France, Portugal, and Poland challenges, with an October 2026 trial.
  • Lynparza faces Canadian generics in October 2026, threatening near-term ovarian-cancer revenue.
  • Tagrisso and Forxiga patent losses would puncture AstraZeneca's cash engines before 2027.

What makes AstraZeneca unique

  • Sept. 28, 2026 Summit deal extends AstraZeneca's ADC leadership into PD-1/VEGF combinations.
  • July 2026 CLARITY-Gastric01 strengthened sonesitatug vedotin, reinforcing AstraZeneca's GI oncology franchise.
  • Sept. 25, 2026 baxdrostat registration shows durable cardiovascular depth beyond oncology.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

401(k) Retirement Plan

Paid Vacation

Paid Holidays

Flexible Work Hours

Growth & Insights and Company News

Headcount

6 month growth

↑ 6%

1 year growth

↑ 6%

2 year growth

↑ 9%
MedCity News
Sep 29th, 2026
AstraZeneca places a $2B bet on a Summit Therapeutics cancer drug.

AstraZeneca places a $2B bet on a Summit Therapeutics cancer drug. AstraZeneca's equity investment in Summit Therapeutics comes with plans for clinical trial collaborations. The deal brings AstraZeneca into a growing group of pharmaceutical companies testing the pairing of antibody drug conjugates with PD-1/VEGF bispecific antibodies, a drug combination that could offer advantages in cancer treatment. By Frank Vinluan on September 29, 2026 3:25 pm AstraZeneca is making a $2 billion equity investment in Summit Therapeutics, a business deal that also kicks off a research collaboration that could pursue multiple drug combinations with an initial focus on gastrointestinal cancers. The deal announced after Monday's market close is a vote of confidence in the Summit cancer drug ivonescimab, a bispecific antibody designed to bind to two targets, PD-1 on T cells and VEGF on cancer cells. Several oncology-focused pharmaceutical companies have already struck deals to add such drugs to their pipelines. Summit's late-clinical drug gives AstraZeneca access to a contender in the class. Ivonescimab was developed by China-based Akeso Therapeutics. Phase 3 trial results in lung cancer raised hopes for the molecule as data showed it beat Merck's blockbuster PD-1 inhibitor Keytruda in a head-to-head study. But those results were from a trial in China, where the drug has approvals in lung cancers and is marketed by Akeso. For Summit, ivonescimab's prospects ride on the results of clinical trials the company is conducting in outside of China. Summit holds rights to the drug in North and South America, Europe, the Middle East, Africa, and Japan. We are taking a look at how health insurers are using AI, defining success, and managing cybersecurity risks. Give us your opinions by completing our brief, anonymous survey. AstraZeneca is a leader in the development and commercialization of antibody drug conjugates (ADCs) for cancer. The Summit deal gives AstraZeneca the opportunity to test its experimental ADC sonesitatug vedotin (sone-ve) in combination with ivonescimab. In July, AstraZeneca reported sone-ve led to statistically significant improvement in overall survival, meeting the main goal of a Phase 3 test in CLDN18.2-positive gastric cancers. Detailed trial results are scheduled for presentation at the upcoming European Society for Medical Oncology conference in late October. This medical meeting will also include the presentation of data for ivonescimab in biliary tract cancer. Last month, Summit reported preliminary Phase 3 results showing statistically significant improvement. This pivotal study was conducted by Akeso in China. Drug resistance is one limitation of ADCs, but PD-1/VEGF bispecific antibodies may be able to help. In addition to bringing two distinct approaches to cancer, the dual mechanism also makes the tumor microenvironment more favorable to ADCs, which is hoped to overcome resistance. The potential advantages of combining PD-(L)1/VEGF bispecific antibodies with an ADC has led to a flurry of dealmaking to explore such drug pairings. AbbVie, Bristol Myers Squibb, Merck, Pfizer, and have struck business deals for bispecific antibodies in this class. Biotech companies are also striking deals. Late last year, Crescent Biopharma licensed a Kelun Biopharma ADC it plans to test in combination with its PD-1/VEGF bispecific antibody. AstraZeneca's new collaboration could extend beyond sone-ve. The Summit deal includes a non-binding memorandum of understanding that permits additional clinical trials testing ivonescimab in combination with other AstraZeneca cancer drugs, including other ADCs. presented by We have the opportunity to design systems that give people greater capacity for the work where human presence matters most: listening, understanding, reassuring, deciding, and caring. "A core pillar of our oncology strategy is to broaden the reach of our ADC portfolio as the backbone of treatment across tumor types with combinations alongside next-generation immunotherapies," Susan Galbraith, AstraZeneca executive vice president, oncology hematology R&D, said in a prepared statement. AstraZeneca's Summit investment lends additional validation to the class of bispecific PD-(L)1/VEGF antibodies, Leerink Partners analyst Daina Graybosch said in a research note. But she also characterized the deal as "more tepid than an outright acquisition," adding that while the collaboration may lead AstraZeneca to invest more in Summit, it's also possible the pharma company learns from the trials and then licenses a competing drug in the class. That strategy has precedent. Graybosch pointed to a TROP2-targeting ADC that Merck licensed from Kelun. The deal happened after Merck reviewed data from clinical trials it conducted in collaboration with AstraZeneca and Gilead Sciences. Astrazeneca's agreement with Summit calls for the pharma company to buy about 108,955 shares of its new partner for $18.36 each, representing an 18.6% premium over Monday's closing stock price. The companies will jointly contribute to the costs of the planned clinical trials, which they expect will be sponsored by AstraZeneca. Each company also retains development and commercialization rights to its respective molecules. The deal is expected to close by the end of this week.

Affärsvärlden
Sep 29th, 2026
AstraZeneca seeks US approval for lung cancer combination.

AstraZeneca seeks US approval for lung cancer combination. The pharmaceutical company AstraZeneca has submitted an application to the FDA for approval of Orpathys in combination with Tagrisso for locally advanced or metastatic EGFR-mutated lung cancer with MET overexpression or amplification after prior EGFR-directed treatment. Today 11:15 This is stated in a press release from the partner Hutchmed. The application is supported by the phase 3 study SAFFRON, in which the combination improved both progression-free and overall survival compared with platinum-based doublet chemotherapy. Orpathys (with the active substance savolitinib) is being developed jointly through a global collaboration between AstraZeneca and Hutchmed. AstraZeneca 1,677.50 SEK +1.64% (+27.0 SEK)

AstraZeneca
Sep 28th, 2026
AstraZeneca invests $2B in Summit Therapeutics to advance cancer ADC combination strategy

AstraZeneca has announced a $2 billion equity investment in Summit Therapeutics to advance cancer treatment combinations. The investment will give AstraZeneca approximately 12% of Summit's outstanding common stock. The companies have entered a clinical collaboration to evaluate sonesitatug vedotin, a Claudin-18.2 antibody drug conjugate, combined with ivonescimab, a bispecific antibody targeting PD-1 and VEGF, in gastrointestinal cancers. Trials are set to begin imminently. Each company will retain development and commercial rights to their respective medicines whilst jointly contributing to trial costs. The collaboration aims to broaden AstraZeneca's ADC portfolio across multiple tumour types. AstraZeneca recently reported positive results from the CLARITY-Gastric01 trial for sonesitatug vedotin in advanced gastric cancers, with results to be presented at a 2026 medical congress.

MarketScreener
Sep 28th, 2026
Summit Therapeutics Inc. and astrazeneca enter into clinical trial collaboration to evaluate ivonescimab in combination with sonesitatug vedotin in multiple gastrointestinal cancers.

Summit Therapeutics Inc. and astrazeneca enter into clinical trial collaboration to evaluate ivonescimab in combination with sonesitatug vedotin in multiple gastrointestinal cancers. Published on 09/28/2026 at 05:30 pm EDT S&P Capital IQ Summit Therapeutics Inc. entered into a clinical collaboration agreement with AstraZeneca to evaluate sonesitatug vedotin in combination with ivonescimab with the intent to start studies in certain gastrointestinal (GI) cancer settings imminently. Under the terms of the clinical collaboration agreement, each company will contribute their respective compound for the combination studies to be conducted, and the parties will jointly contribute to the costs of such studies, which are intended to be sponsored by AstraZeneca. Each company will retain development and commercial rights to their respective molecules. Moreover, Summit and AstraZeneca intend to evaluate ivonescimab with an additional set of AstraZeneca?s cancer medicines, including other antibody drug conjugates (ADCs). The companies intend to share clinical development costs of potential future studies. Each company will retain their current development and commercial rights to their respective molecules, and the agreement is mutually non-exclusive. There are no additional financial considerations associated with milestones, royalties, revenue-sharing, or profit-sharing. The Memorandum of Understanding with respect to the potential clinical trial collaboration between Summit and AstraZeneca is non-binding, and there can be no assurances that the intended clinical trial collaboration comes to fruition. (C) S&P Capital IQ - 2026

University of Arkansas for Medical Sciences
Sep 25th, 2026
College of Pharmacy recognized at national convention.

College of Pharmacy recognized at national convention. By Benjamin Waldrum Sept. 25, 2026 | The UAMS College of Pharmacy's student chapter of the Student National Pharmaceutical Association (SNPhA) received an award at its annual convention in August, and several pharmacy students were recognized with individual honors. SNPhA is the official student association of the National Pharmaceutical Association (NPhA). Goodlow posing with a placard listing her as a candidate for public relations liaison, for which she was later elected. This year, the UAMS student chapter received an award for 20% membership growth, notable for a smaller chapter. This year's delegates were third-year students Lynn Duncan, Marissa Bones, Ma'Kyah Goodlow, and Mackenzie Rodgers, along with second-year students Tykia Rankin and Bryce Piper-Eason. "It was an incredible experience," Goodlow said. "We all had a wonderful time networking, learning, and representing UAMS on the national stage." Goodlow was elected as the SNPhA national public relations liaison and was a finalist in AstraZeneca's Medical Science Liaison competition. Goodlow, Duncan, and Piper-Eason participated in the CVS Health Leadership Academy. Rodgers was nominated to serve on the Nominations Committee next year, which helps select and vet key leadership positions. "I am incredibly proud to see our students recognized nationally," said Kendrea Jones, Pharm.D., the chapter's co-advisor. "Their accomplishments reflect the mission of SNPhA to support the professional development of pharmacy students while improving the health of underserved communities. These students have demonstrated leadership, professional growth and a commitment to service throughout the year, and their national recognition is a wonderful reflection of their hard work and the strength of our UAMS chapter." Rodgers, the chapter president this year, worked alongside representatives from around the country to vet candidates for the SNPhA National Executive Board, including candidates from Region 4, which includes Arkansas. "I am incredibly blessed and grateful to serve on this committee engaging with the future pharmacists of the nation," Rodgers said. "I'm thankful for the many connections made at the conference and highly encourage students to take any opportunity to attend a conference at least once throughout your academic career - you never know who you will meet."