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Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Counsel – AI Governance - Law and Compliance

Full-TimeUpdated on 10/23/2026Deadline 1/30/27
$202.1k - $269.3k+ Discretionary incentive cash + Stock opportunities
Senior
JD
Cambridge, MA, USA+5 moreMore locations: Washington, DC, USA | Madison, NJ, USA | Princeton, NJ, USA | Brisbane, CA, USA | San Diego, CA, USA
In PersonRole is marked hybrid; the posting does not specify the office/home-day schedule.
LegalLegal Counsel & Legal Support
Company Historically Provides H1B Sponsorship

About the job

Requirements
  • A Juris Doctor or equivalent legal degree and active bar membership in at least one U.S. jurisdiction are required.
  • The role requires 5–7 years of combined legal experience at a top law firm or in-house.
  • The role requires at least 2 years of substantive experience in AI legal and compliance or AI governance.
  • Working knowledge of the EU AI Act, NIST AI Risk Management Framework, ISO/IEC 42001, OECD AI Principles, and U.S. federal and state AI guidance is required.
  • Ability to translate complex regulatory requirements into pragmatic, business-aligned guidance is required.
  • Strong drafting, analytical, and stakeholder management skills are required, along with the ability to work independently in a fast-moving, cross-functional environment.
  • Sound judgment and discretion in handling novel, ambiguous, and high-visibility issues are required.
Responsibilities
  • Provide legal counsel on AI initiatives across the AI lifecycle, including intake review, risk classification, model development, deployment, monitoring, and decommissioning.
  • Conduct and document AI legal risk assessments covering intellectual property, privacy, bias and fairness, transparency, safety, accountability, and third-party risk.
  • Support implementation of the enterprise AI governance framework, including model inventory, lifecycle controls, human oversight protocols, and incident response workflows.
  • Track and interpret global AI laws, regulations, guidance, and standards, and translate them into actionable policies, playbooks, standards, and training materials.
  • Review and negotiate AI-related contractual provisions with vendors, partners, and customers, including data use, model training, indemnities, and audit rights.
  • Advise on generative AI and high-risk AI use cases across research and development, commercial, medical, manufacturing, and enabling functions.
  • Partner with Privacy Law & Compliance on automated decision-making, profiling, cross-border data transfers, and data subject rights.
  • Support engagement with regulators, industry groups, and standards bodies, and contribute to internal thought leadership on responsible AI.
  • Help design and deliver AI governance and compliance training for legal, compliance, and business audiences.
  • Maintain clear documentation to support audit readiness, regulatory inquiries, and governance maturity assessments.
Desired Qualifications
  • CIPP (such as CIPP/US or CIPP/E) and/or IAPP AIGP certification is preferred.
  • Prior experience in the pharmaceutical, biotechnology, healthcare, or life sciences industry is preferred.
  • Familiarity with privacy laws and frameworks, including GDPR, HIPAA, CCPA/CPRA, and China PIPL, and their intersection with AI is preferred.
  • Experience with AI assurance artifacts such as model cards, system cards, and impact assessments, and with governance tooling is preferred.
  • A working understanding of machine learning concepts, data science workflows, and digital product development is preferred.
  • Experience supporting third-party/vendor AI risk reviews and contracting is preferred.
  • Engagement with industry working groups, standards bodies, or responsible AI forums is preferred.
  • Comfort using AI-enabled tools to enhance legal workflows and efficiency is preferred.

About the company

Bristol Myers Squibb discovers, develops and sells prescription medicines for serious illnesses, including cancer, blood disorders, immune diseases and heart disease, for patients treated by doctors and hospitals around the world. Its best-known drug is Opdivo, an immunotherapy that helps the body's own immune system find and attack many kinds of cancer. Researchers develop drug candidates in its labs or bring them in through acquisitions and partnerships, then test them in clinical trials to win regulatory approval. The company makes and markets the approved medicines and earns its revenue from sales of patent-protected drugs. Its roots go back to a business founded in 1887, and it is based in Lawrence Township, New Jersey.

Company Size

10,001+

Company Stage

IPO

Headquarters

Lawrence Township, New Jersey

Founded

1887

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Simplify's Take

What believers are saying

  • Sales are beating forecasts: BMS raised 2026 revenue guidance to $49 billion to $50 billion in July 2026.
  • Newer drugs carry the business: they made $7.6 billion of $13.0 billion in sales in the June 2026 quarter.
  • Manufacturing careers are expanding: a $2.3 billion Houston campus announced in August 2026 will add nearly 500 skilled roles.

What critics are saying

  • Job security is shaky: BMS added 265 New Jersey layoffs in September 2026, bringing its 2026 state cuts to 718.
  • A patent cliff looms: Eliquis and Opdivo, its two biggest drugs, lose US exclusivity around 2028.
  • Older drugs are shrinking fast: Revlimid sales fell 49% to $425 million in the June 2026 quarter as generics spread.

What makes Bristol Myers Squibb unique

  • BMS owns a psychiatry first: Cobenfy treats schizophrenia without blocking dopamine, unlike antipsychotics used for decades.
  • Its top seller is shared: BMS splits Eliquis blood thinner profits roughly equally with Pfizer in most markets.
  • BMS reengineers patients' own immune cells: it sells two CAR T therapies, Breyanzi and Abecma, for blood cancers.

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Benefits

  • Flexible Work Hours
  • Hybrid Work Options
  • Professional Development Budget

Growth & Insights and Company News

Headcount

6 month growth

8%

1 year growth

7%

2 year growth

7%
Market Chameleon
Oct 19th, 2026
Bristol Myers to bring 12 oral presentations and nearly 60 oncology disclosures to ESMO 2026.

Bristol Myers to bring 12 oral presentations and nearly 60 oncology disclosures to ESMO 2026. 19 October 2026, 8:50 AM By Market Chameleon Produced with AI assistance and reviewed by Market Chameleon staff. Bristol Myers Squibb (BMY) said it will present new data across its oncology portfolio and pipeline at the European Society for Medical Oncology (ESMO) 2026 Congress (October 23-27 in Madrid), spanning 12 oral presentations and nearly 60 disclosures. The company's update spotlights multiple modalities across solid tumors, including late-breaking Phase 3 studies for izalontamab brengitecan (iza-bren) and late-breaking global Phase 2 data for pumitamig, alongside long-term survival results for Opdivo plus Yervoy. ESMO 2026 presence emphasizes late-breaking Phase 3 and Phase 2 catalysts across solid tumors. In the announcement, Bristol Myers highlighted two late-breaking, Phase 3 studies of izalontamab brengitecan (iza-bren), described as a potential first-in-class EGFR x HER3 bispecific antibody-drug conjugate (ADC), in EGFR-mutated non-small cell lung cancer (PANKU-Lung01) and HR+/HER2- breast cancer (PANKU-Breast01).

Savills
Oct 14th, 2026
San diego Q3 2026 life sciences market report.

San diego Q3 2026 life sciences market report. 14 October 2026 Market highlights. * Overall vacancy increased 60 basis points year over year to 28.5% in Q3 2026, up from 27.9% in Q3 2025. The increase was driven by direct vacancy, which rose to 25.8%, while sublease vacancy declined to 2.8%. * Venture capital funding slowed considerably in 2026, with $1.4 billion raised across 113 deals through Q3, down 34.1% year over year and marking the lowest Q1 through Q3 total since 2022. * Alexandria Real Estate delivered a 427,000-square-foot R&D hub for Bristol Myers Squibb at Campus Point, establishing the company as an anchor tenant at the 2.9- million-square-foot life sciences campus.

Yahoo Finance
Oct 13th, 2026
Eli Lilly beats Bristol Myers Squibb on growth: $65.2B revenue, 45% rise vs. $48.2B

A comparison of Bristol Myers Squibb and Eli Lilly concludes that Lilly is the better healthcare stock to buy in 2026, even at a premium. Lilly's 2025 revenue rose about 45% to $65.2 billion, with net income near $21 billion. Bristol Myers' revenue slipped 0.2% to $48.2 billion, though it returned to a net income of $7.1 billion after an $8.9 billion loss in 2024. Lilly trades at 33.8 times forward earnings against 8.2 times for Bristol Myers. The article says Bristol Myers is cheap for good reason, citing pricing pressure, patent expiries, and an unpredictable recovery. Lilly's weight-loss drugs Zepbound and Mounjaro are expected to lift 2026 revenue above 30%, to $88.6 billion. Bristol Myers is forecast to grow 3% to $49.9 billion.

Chinese LGZ
Oct 9th, 2026
Bristol Myers Squibb unveils $2.3 billion investment in cutting-edge Houston pharma facility.

Bristol Myers Squibb unveils $2.3 billion investment in cutting-edge Houston pharma facility. Source link: https://houston365.info/2026/10/09/bristol-myers-squibb-unveils-2-3-billion-investment-in-cutting-edge-houston-pharma-facility/ Bristol Myers Squibb strengthens Houston's life sciences sector with $2.3 billion facility. Bristol Myers Squibb is set to transform Houston's pharmaceutical landscape through a landmark $2.3 billion investment in a cutting-edge manufacturing plant. This initiative, developed in collaboration with the Greater Houston Partnership, aims to elevate the company's production capabilities while cementing Houston's status as a burgeoning center for biopharmaceutical innovation. The project is projected to generate hundreds of skilled jobs and stimulate substantial economic growth within the region. Project overview and strategic importance. The new facility will incorporate the latest manufacturing technologies to optimize efficiency and product quality. With over 1,200 new roles anticipated in scientific research, engineering, and production, the plant will serve as a catalyst for workforce development and community engagement. This expansion aligns with Bristol Myers Squibb's vision to accelerate the delivery of novel therapies and reinforces Houston's growing influence in the life sciences ecosystem. * Innovative manufacturing processes: Adoption of advanced automation and quality control systems. * Employment opportunities: Creation of more than 1,200 specialized jobs across multiple disciplines. * Community collaboration: Strengthening partnerships with local universities and healthcare institutions to foster innovation. | Investment Detail | Information | | Total... | - - Author: Samuel Brown Publish date: 2026-10-09 15:23:00 Copyright for syndicated content belongs to the linked Source. - - 1 - 2 - 3 - 4 - 5 - 6 - 7 - 8

GlobeNewswire
Oct 6th, 2026
Sotyktu gains ground in Psoriatic Arthritis, but rheumatologists remain selective as its role in the treatment algorithm takes shape, according to Spherix Global Insights.

Sotyktu gains ground in Psoriatic Arthritis, but rheumatologists remain selective as its role in the treatment algorithm takes shape, according to Spherix Global Insights. New research finds growing prescriber adoption and enthusiasm for TYK2 differentiation, while limited experience, access friction, and questions around joint efficacy temper early launch momentum. Exton, PA, Oct. 06, 2026 (GLOBE NEWSWIRE) - Five months into the U.S. launch of Bristol Myers Squibb's (BMS) Sotyktu (deucravacitinib) for psoriatic arthritis (PsA), rheumatologists are increasingly adding the oral TYK2 inhibitor to their treatment armamentarium. Yet, new research from Spherix Global Insights suggests that broader trial has not yet translated into deep utilization, as physicians continue to refine where Sotyktu fits within an already crowded PsA treatment landscape. Findings from Spherix's latest wave of Launch Dynamix(TM): Sotyktu in Psoriatic Arthritis (US) reveal that 41% of rheumatologists have now prescribed Sotyktu, approximately double the proportion observed shortly after launch. However, depth of use remains limited, with new patient initiations slowing to their lowest level since launch and rheumatologists becoming increasingly selective in the proportion of PsA patients they consider appropriate candidates for the therapy. The pattern suggests that rheumatologists are willing to trial Sotyktu, but are doing so selectively as they gain experience with the product. Importantly, physicians have not written off the drug's longer-term potential. Despite selective use today, rheumatologists continue to anticipate a meaningful role for Sotyktu once fully established, with expectations holding relatively steady throughout the early launch period. A New Oral Option Is Finding Its Niche Sotyktu's novel TYK2 mechanism of action and expected efficacy remains the leading drivers of initiation, with its oral administration and perceived safety profile creating particular appeal for patients who wish to avoid injections or for whom JAK inhibitors may be less desirable. Indeed, nearly two-thirds of rheumatologists believe Sotyktu will expand their overall use of oral therapies in PsA, rather than simply replace another oral agent. This positioning is beginning to translate into a recognizable patient profile. Current Sotyktu use remains concentrated in moderate disease and third-line-or-later treatment, but first-line use has doubled since May, suggesting that some physicians are beginning to experiment with the drug earlier in the treatment journey. The result is an emerging position for Sotyktu somewhere between Otezla and traditionally more potent advanced therapies, an oral option that may appeal both to earlier patients seeking to avoid injectable biologics and to more heavily pretreated patients in need of another mechanism. "I've been using it, like a first-line agent, kind of like a stronger Otezla that has better data." one rheumatologist told Spherix. TYK2 Differentiation Resonates, but Joint Efficacy Remains a Question Rheumatologists appear to recognize meaningful differentiation in Sotyktu's TYK2 mechanism, with its oral profile, perceived safety, and efficacy contributing to an emerging position within the PsA treatment landscape. Early perceptions suggest the therapy may occupy a distinct space among existing oral and advanced treatment options without directly mirroring the profile of any one competitor. At the same time, early clinical experience is introducing some nuance. While physicians report positive experiences among many patients treated to date, questions around joint efficacy relative to established advanced therapies remain, suggesting that greater real-world experience may be important in determining how broadly rheumatologists ultimately use Sotyktu. A Quiet Launch May Be Limiting Momentum Beyond product perceptions, Spherix's findings point to commercial execution as another potential constraint on uptake. More than half of rheumatologists report that they have never interacted with a BMS sales representative for Sotyktu in PsA, and physicians interviewed by Spherix frequently characterized BMS's launch presence as relatively quiet compared with other recent rheumatology launches. Access also remains a friction point. Among recent Sotyktu initiations, 81% required prior authorization, although most were approved on the first attempt. TNF inhibitor failure remains the most common payer requirement. More broadly, rheumatologists' perception of Sotyktu access has become somewhat more restrictive since launch, with nearly one-third now characterizing payers as restricting access. Experience May Be the Next Inflection Point For now, Sotyktu appears to have cleared an important early hurdle: physicians are trying it. The next challenge will be converting that breadth of trial into greater depth of use. Limited familiarity and clinical experience remain the most frequently cited barriers to increased prescribing, while concerns about efficacy, particularly in more severe joint disease, have become more prominent as rheumatologists accumulate experience. Still, Sotyktu's differentiated mechanism, oral administration, and perceived safety advantages give the brand multiple potential paths to growth. With physicians continuing to project meaningful longer-term use, the coming months will help determine whether Sotyktu remains a selectively used alternative or establishes a broader role between Otezla and higher-potency advanced therapies. Launch Dynamix(TM): Sotyktu in Psoriatic Arthritis (US) is an independent Spherix Global Insights service tracking the launch of Sotyktu among U.S. rheumatologists. The August Deep Dive is based on quantitative research with 78 rheumatologists conducted August 5-8, 2026, supplemented by qualitative interviews with six rheumatologists conducted August 24-28. Launch Dynamix provides monthly benchmarking during the first 18 months of commercial availability, augmented by quarterly deep dives examining patient types, brand perceptions, promotional activity, and drivers and barriers to uptake. About Launch Dynamix(TM) Launch Dynamix(TM) is an independent service providing monthly benchmarking of newly launched products for the first eighteen months of commercial availability, augmented by a quarterly deep dive into promotional activity, barriers to uptake, and patient types gravitating to the launch brand. About Spherix Global Insights Spherix Global Insights is a leading independent provider of market intelligence and advisory services for specialty pharmaceutical and biotech markets. By combining physician, patient, and payer perspectives into an integrated view, Spherix helps brand teams, market access stakeholders, and investors understand how a specialty market actually behaves, not how any one stakeholder describes it. The firm operates ten dedicated therapeutic franchises - Dermatology, Gastroenterology, Hematology, Nephrology, Neuroscience, Obesity, Oncology, Ophthalmology, Respiratory and Rheumatology - plus a Market Access team. Each franchise is staffed by hyper-focused experts who track these markets full-time, drawing on independently curated communities of vetted specialists, patients, and payers to deliver quarterly trending, launch tracking, chart audits, and KOL synthesis. Trusted by 19 of the top 20 pharmaceutical and biotech organizations, Spherix has been a go-to resource for more than a decade for leading brands, industry media, financial analysts, and patient advocacy groups. To learn more about Spherix Global Insights, visit spherixglobalinsights.com or connect through LinkedIn. For more details on Spherix's primary market research reports and interactive dashboard offerings, visit or register here: https://clientportal.spherixglobalinsights.com.