AstraZeneca Posted October 5, 2026

Associate Director, AI for Oncology Clinical Development

Cambridge, Massachusetts, United States of America Full time
Clinical Development Oncology Associate Director
Notify me about similar jobs

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

Drug discovery has benefitted enormously in the current AI era yet comprises only a portion of the journey to bring new treatments to those in need. The final step – clinical drug development – is oft overlooked, despite requiring a significant proportion of time and investment. In the AI for Clinical Development team at AstraZeneca, we're reimagining the process of clinical development. Our vision is to bring safe, efficacious treatments to patients in a way that quantifiably improves our chance to do this faster, more cost-effectively, and with reduced patient burden.

In this role, you will be a technical lead to help us leverage the power of AI to the fullest, alongside our other computational, statistical, and machine learning tools. You will work across the enterprise to define and deliver on AstraZeneca’s most pressing clinical development questions. You will proactively collaborate in cross-functional teams spanning AstraZeneca’s key Oncology foci of hematology, cell therapy, antibody-drug conjugates, small molecules, and biologics. This is an unprecedented, high visibility opportunity to invent new ways to leverage data, models, and learnings across the spectrum of cancer biology and drug modalities – and importantly, you and the team will apply these new methods to measurably advance the late-stage drug pipeline and our group’s ambition.

Responsibilities:

Contribute to the AI strategy and roadmap for Oncology early and late phase clinical development

Serve as a key technical lead and contributor in matrixed teams to deliver complex, high-stakes AI projects

Evaluate and develop cutting-edge AI methods in one or more areas of problem definition, data considerations, governance, algorithm development, validation, and adoption

Partner with clinical development, biometrics, regulatory, and study teams to develop and then validate novel AI solutions into clinical study design, execution, strategy, and decision-making

Establish and maintain external collaborations with academic institutions, technology partners, and industry consortia to access novel capabilities and advance the AI roadmap

Represent AstraZeneca at scientific conferences, standards bodies, and peer-reviewed venues; contribute first- or last-author publications in leading ML and clinical AI journals

Mentor and support peers within the team

Qualifications:

PhD in a quantitative discipline such as computer science, bioinformatics, computational biology, mathematics, physics, biophysics, computational neuroscience, biostatistics

At least 2+ years’ work experience outside of PhD with measurable impact (e.g. models delivered, patents, SaMD filings, first-author publications, open-source projects, standards-body participation)

Technical requirements:

Exceptional software development and coding skills, leveraging frontier coding agent frameworks; knowledge of computing hardware a plus

Deep experience, knowledge, and understanding of one or more fields of biology

Deep understanding of machine learning fundamentals, with domain expertise in one or more of the following - Training and tuning foundation models

Bayesian inference

Temporal modeling

Multimodal integration and modeling

Model calibration and domain adaptation

Data-centric AI: acquiring, creating, and curating datasets for model training / post-training / benchmarking / evals

Model and data evaluations and benchmarking

Model interpretability

Model post-training and alignment

Preferred Skills:

Deep expertise in cancer biology

Experience working with biological data such as molecular (e.g. DNA, RNA, protein), imaging (radiology, microscopy), or clinical text (e.g. EHR, clinical notes)

Experience in drug development including but not limited to clinical trial design, biomarker discovery, companion diagnostics, dosing, safety, endpoints, and regulatory

Experience in a matrixed global organization spanning multiple sites and therapy areas

Up to date with the latest AI research and tools, proactively trying out those of interest, and ability to discern hype from true added value

The annual base pay for this position ranges from $144K to $216K. 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.

Date Posted

05-Oct-2026

Closing Date

11-Oct-2026 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
Associate Director
Function
Clinical Development
Therapeutic area
Oncology
Location
Cambridge, Massachusetts, 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 567 comparable Associate Director Clinical Development roles across 75 biopharma companies.

567Comparable roles tracked
504Currently active
75Companies hiring similar roles
46Countries represented

Salary context

174 of 567 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 · Sr Site Activation Coordinator · IQVIA $35,800/yr – $102,000/yr
Highest disclosed · Sr Statistical Advisor · Gilead Sciences, Inc. $261,375/yr – $338,250/yr
Peer group range $68,900 – $299,813 (median $176,800)

Where these roles are based

Top locations among the 567 comparable roles

United States245
India70
United Kingdom36
Spain22
China18
Poland18

+ 40 more countries

Seniority mix

567 of 567 peers have a known seniority level

Manager288
Senior149
Associate Director130

Therapeutic area mix

50 of 567 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology27
Immunology8
Neuroscience6
Respiratory2
Ophthalmology2
Gastroenterology2
Dermatology & Aesthetics2
Cardiovascular / CVRM1

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.

100%similar
Eisai Inc. US Field Based, United States Associate Director
Same function Same therapeutic area Same seniority Same country
100%similar
Eisai Inc. New Jersey, United States Associate Director
Same function Same therapeutic area Same seniority Same country
100%similar
AbbVie North Chicago, IL Associate Director
Same function Same therapeutic area Same seniority Same country
100%similar
AbbVie Associate Director
Same function Same therapeutic area Same seniority Same country

Open in 2 locations

Waltham, United StatesSouth San Francisco, United States
100%similar
ModernaTX, Inc. Cambridge, United States Associate Director
Same function Same therapeutic area Same seniority Same country
100%similar
Eisai Inc. US Field Based, United States Associate Director
Same function Same therapeutic area Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Clinical Development job in the United States, and choose locations and companies.

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.

100%
Associate Director or Director, Medical Science Liaison, Oncology - Northeast and Mid-Atlantic region / Field-based
Eisai Inc. · US Field Based, United States · Associate Director
Function Therapeutic area Seniority Country
100%
Associate Director, Clinical Pharmacology/Senior Clinical Pharmacologist (Oncology)
AbbVie · Waltham, MA · Associate Director
Function Therapeutic area Seniority Country
100%
Associate Director or Director, Medical Science Liaison, Oncology – West Region / Field-based
Eisai Inc. · US Field Based, United States · Associate Director
Function Therapeutic area Seniority Country
90%
Senior Clinical Pharmacologist (Oncology)
AbbVie · San Francisco, CA · Senior
Function Therapeutic area Adjacent seniority Country
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.