Location: Wilmington, DE
Date Posted: 03/25/2026
AstraZeneca Overview
AstraZeneca is a global, science-led biopharmaceutical company focusing on the discovery, development, and commercialization of prescription medicines for some of the world’s most serious diseases. We push the boundaries of science to deliver life‑changing medicines to patients across our key therapeutic areas.
We have an exciting opportunity for a talented, pragmatic, and intellectually curious lawyer to support our US and global teams in the BioPharmaceuticals Business Unit. The role will operate under the supervision of the Deputy General Counsel and provide legal support to business teams across three therapeutic areas: Respiratory & Immunology; Cardiovascular, Renal & Metabolism; and Vaccines & Immune Therapies.
The role is based in our US Sales & Marketing headquarters in Wilmington, DE.
About the Role
The Senior Counsel plays two important roles within the BioPharmaceuticals Legal team. First, the Senior Counsel is responsible for the strategy, management, and budgeting of global litigation and government investigation matters. Second, the Senior Counsel will be a proactive business partner advising on key legal risks and opportunities across the product lifecycle.
Critical thinking and influencing skills are key, as the position has a direct impact on business activities with significant reputational or financial value and risk. The Senior Counsel must be able to articulate legal considerations to business stakeholders clearly and concisely with a strong understanding of internal and external legal trends.
Areas of experience should include intellectual property litigation in the pharmaceutical space before a federal court and, ideally, before administrative tribunals. Candidates with experience in product liability litigation, contract evaluation and dispute resolution, along with the US pharmaceuticals regulatory and compliance framework—specifically the US False Claims Act and Anti‑Kickback Statute—are also encouraged to apply.
Main Duties and Responsibilities
- Independently lead IP litigations, contract disputes, product liability litigations, as well as government investigation matters.
- Effectively partner with outside counsel and internal AstraZeneca stakeholders on strategies to bolster litigation positions and facilitate the ability of the BioPharmaceuticals business to achieve its objectives.
- Establish appropriate litigation matter budgets and ensure costs are delivered within acceptable budget variances.
- Coordinate timely and practical advice on commercial regulatory and litigation risks across assigned BioPharmaceuticals therapy areas.
- Advise on legal aspects of contractual arrangements and strategic opportunities with customers and partners.
- Advise on mitigation strategies for fraud and abuse and other legal risks related to market access and commercial strategies for assigned products.
- Work effectively with individuals at all levels of the organization and collaborate on legal advice within the broader legal team.
- Demonstrate leadership within business and legal teams by proactively seeking to improve ways of working and contribute to the professional development of colleagues.
Essential Requirements
- Law degree and admission to the bar of at least one state.
- 5+ years of experience working in the legal department of a corporation or major law firm, preferably within the pharmaceutical industry.
- Experience handling sophisticated IP disputes.
- Experience preparing pleadings, motions, and discovery responses in IP litigation matters.
- Ability to take accountability, appropriately calibrate risk, and enable clear decision‑making with confidence and professional maturity.
- Intellectually curious, with an appetite for learning and a proven ability to master new subjects quickly and effectively.
- Ability to work flexibly and collaboratively, maintain positive relationships, and manage a diverse workload.
- Excellent interpersonal, communication, and presentation skills, with the ability to operate effectively under pressure.
- High level of integrity and strong work ethic.
Highly Desirable Requirements
- In‑depth understanding of US drug pricing and reimbursement processes and experience advising on associated risks.
- Experience in US pharmaceutical regulatory and compliance frameworks, specifically the US False Claims Act and Anti‑Kickback Statute.
- Experience in product liability litigation.
- Experience in contract evaluation and dispute resolution.
Why Join Us?
When we put unexpected teams in the same room, we fuel ambitious 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 bold world.
AstraZeneca offers an environment where your expertise can truly shine. Here, you’ll be part of a community of dedicated scientists who are both encouraging and challenging. We embrace global opportunities across all Therapy Areas, pushing boundaries to deliver ground‑breaking solutions. Our collaborative approach ensures that every opinion is valued, fostering an inspiring learning environment where setbacks are seen as opportunities for growth. With countless learning opportunities and a dedication to making a profound impact on society and patients worldwide, AstraZeneca is where you can apply your skills in innovative ways.
Ready to take the next step in your career? Apply now to join our dynamic team!
Equal Opportunity Statement
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.
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