B

Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Senior Manager - Business Analyst & Scrum Master

Full-TimeUpdated on 10/23/2026Deadline 12/28/26
$150.1k - $181.9k+ Discretionary incentive cash + Stock opportunities
Expert
Bachelor's
Princeton, NJ, USA
In Person
IT OperationsEnterprise Applications
Company Historically Provides H1B Sponsorship

About the job

Requirements
  • A bachelor's degree in Business, Information Technology, Life Sciences, or a related field is required; an advanced degree is a plus.
  • Typically 10+ years of relevant business analysis, delivery, or IT experience, including demonstrated experience directly managing teams in a global or matrix environment.
  • Specialized, hands-on experience with field sales force platforms, such as Veeva CRM, territory alignment, call planning, sample management, or incentive compensation systems, is required.
  • Proven experience as a Scrum Master or agile delivery lead, with the ability to establish and scale agile practices across a delivery team.
  • Demonstrated people-leadership skills, including goal-setting, coaching, performance management, and meaningful input into hiring, promotion, and compensation decisions.
  • A strong background in requirements elicitation, process mapping, and documentation (business requirements documents, functional specifications, and user stories), with the ability to guide and quality-check a team's output.
  • Proficiency in Jira for backlog and sprint tracking is expected.
  • Pharma commercialization experience is required, with direct exposure to field sales operations and supporting platforms.
Responsibilities
  • Lead and support delivery for the field sales force platform portfolio, including Veeva CRM, orchestration, territory management, call planning, and incentive compensation systems.
  • Own delivery leadership for one or more Sales Systems programs, coordinating business analysis, Scrum, development, and vendor teams to deliver requirements, agile delivery, and platform governance outcomes.
  • Partner with sales operations and field leadership to shape the platform roadmap, align cross-functional delivery teams, and remove obstacles that put program timelines at risk.
  • Own the requirements strategy for field sales force platforms and oversee the business analysis team's elicitation, documentation, and validation of business requirements.
  • Ensure the team's functional specifications, process maps, data mappings, and user stories are clear, traceable, and sprint-ready before delivery.
  • Guide current-state and future-state process analysis for field sales workflows, identifying gaps, inefficiencies, and platform enhancement opportunities.
  • Ensure business requirements documentation is owned, maintained, and traceable from requirement through delivered feature.
  • Oversee Scrum ceremonies and agile delivery practices across field sales platform teams, ensuring consistent and effective application of agile methodology.
  • Maintain oversight of sprint boards and delivery tracking in Jira, ensuring stakeholders can see progress on platform initiatives.
  • Establish and refine standard operating practices for backlog grooming, prioritization, and sprint readiness.
  • Maintain a strategic cross-platform view of field sales force technology and its support for representative-facing and field leadership workflows.
  • Partner with platform administrators and vendors, including Veeva and Salesforce, to evaluate proposed changes for feasibility, downstream data impact, and field user experience.
  • Define and drive the field sales platform roadmap, recommending improvements based on field feedback, usage data, and industry best practices.
  • Serve as the primary point of accountability and trusted business partner to sales operations, field leadership, and commercial stakeholders for platform initiatives.
  • Represent Commercialization BI&T in senior stakeholder discussions and align sales operations, field leadership, data teams, and technical delivery teams around platform priorities.
  • Provide regular structured updates to PMO leadership, sales operations, and senior management on requirements status, delivery progress, risks, and issues.
  • Facilitate retrospectives and requirements-review sessions to improve business analysis practice and delivery execution.
  • Establish and refine standards for business analysis and field sales platform delivery to increase efficiency and data quality.
  • Own reporting on requirements delivery, platform adoption, and data quality metrics for the field sales platform portfolio.
  • Identify requirements gaps, data risks, and platform issues that may affect field sales operations; develop and drive mitigation plans and escalate urgent operational risks.
  • Prepare and present business analysis findings and delivery progress reports to PMO leadership, sales operations, and senior management.
Desired Qualifications
  • Experience with OnePlan or similar project portfolio management tools is a plus.

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

6 month growth

8%

1 year growth

7%

2 year growth

7%
Yahoo Finance
Oct 23rd, 2026
Three defensive stocks to buy as AI selloff hits: BMY, Colgate and Gilead offer dividends

As investors question the costs and returns of the AI boom, some are turning to defensive stocks in healthcare and consumer goods. Three that pay quarterly dividends stand out: Bristol Myers Squibb, Colgate-Palmolive, and Gilead Sciences. Bristol Myers Squibb shares are up 14.3% this year, with a forward dividend yield of 4.3% and 18 straight years of increases. Second-quarter revenue reached $13 billion, with newer products making up nearly 60%. Colgate-Palmolive is up 20.2% this year and has raised its dividend for 64 years in a row. It reported second-quarter revenue of $5.36 billion. Gilead shares have gained 26%, against 13% for the S&P 500. Second-quarter HIV sales rose 12% to $5.7 billion.

MarketScreener
Oct 23rd, 2026
Tempus AI expands Bristol Myers partnership with multi-year oncology, AI data deals.

Tempus AI expands Bristol Myers partnership with multi-year oncology, AI data deals. Published on 10/23/2026 at 10:32 am EDT - Modified on 10/23/2026 at 10:37 am EDT By Adriano Marchese Tempus AI signed a multi-year deal with Bristol Myers Squibb to license oncological data and provide access to its artificial intelligence-powered platform. Under the terms of the deal, Bristol Myers will gain access to Tempus's Lens Platform, the company's agentic AI platform for oncology drug development, which is built on real-world multimodal datasets. The agreement will run through 2031 to support biological and clinical insight, novel drug target discovery and therapeutic development across the pharmaceutical company's oncology portfolio. Additionally, clinical-stage technology firm Pathos AI is also broadening its strategic collaborations with both Bristol Myers and Tempus AI. The collaboration aims to build a specialized, curated dataset and agentic AI capabilities for Alzheimer's disease and other neurological conditions. Bristol Myers led a $237 million Series E financing round for Pathos at a $3 billion valuation, gaining rights to Pathos' Foundry AI platform and broader portfolio. According to a regulatory filing on Friday, the combined agreements provide Tempus with $192.5 million in total cash commitments over five years, consisting of $137.5 million directly from Bristol Myers, and $55 million from Pathos AI for 500,000 de-identified patient records. Write to Adriano Marchese at [email protected] (END) Dow Jones Newswires 10-23-26 1031ET (C) Dow Jones - 2026

941 The Duke
Oct 23rd, 2026
Pathos AI teams up with Bristol Myers and Tempus AI to advance drug development.

Pathos AI teams up with Bristol Myers and Tempus AI to advance drug development. By Thomson Reuters Oct 23, 2026 | 9:00 AM Oct 23 (Reuters) - Pathos AI said on Friday it had entered into a collaboration with Bristol Myers Squibb and Tempus AI to develop artificial intelligence tools for drug development in Alzheimer's disease and other neurological disorders. Pathos AI also raised $237 million in a Series E funding round led by Bristol Myers that valued the New York-based company at about $3 billion, with participation from existing investors. Here are some other details: - Tempus will build a dataset from hundreds of thousands of patients with neurological disorders to help track outcomes and speed research into disease biology - Pathos will license the data from Tempus under a five-year, $55 million agreement - Pathos will apply its AI platform, Pathos Foundry, to study the dataset at scale, generate and test hypotheses on disease biology, and inform the design of more targeted, adaptive clinical trials - Bristol Myers will gain non-exclusive strategic access to Pathos Foundry across its broader portfolio, as well as three-year exclusive rights to use the platform for its neuroscience development programs - Proceeds from the financing will be used to further scale the Foundry platform's capabilities and accelerate development of its AI-driven pipeline, including advancing experimental cancer drug, JSKN016 - The funding will help advance development of other cancer programs including an AstraZeneca-partnered experimental breast cancer drug (Reporting by Sriparna Roy in Bengaluru; Editing by Maju Samuel)

BioPharma Watch
Oct 22nd, 2026
IHI and Bristol Myers Squibb launch National collaborative to expand access to cancer clinical trials.

IHI and Bristol Myers Squibb launch National collaborative to expand access to cancer clinical trials. Key Takeaway: The Institute for Healthcare Improvement and Bristol Myers Squibb launched a three-year initiative to enhance access to oncology clinical trials. The Cancer Collective Action Collaborative aims to address barriers faced by underrepresented populations, particularly in lung and breast cancer. The initiative will involve 24 teams working to improve patient engagement and trial participation. Price reaction · baseline $61.12 (2026-10-21 close) · hit pre-market · clean, no other BMY news in the window day 0 close · peak Market sentiment analysis. Positive factors. * Collaboration aims to improve access to cancer trials. * Focus on addressing disparities in trial participation. * Engagement with diverse healthcare stakeholders. * Evidence-based strategies for sustainable change. BiopharmaWatch analysis. From its catalyst data and publicly available data · not financial advice Best trade, last catalyst 120-day peak, hindsight Typical move average across 15 past catalysts Lead asset Phase 1 · Multiple Myeloma Three-year initiative will bring clinical research closer to patients and address barriers to trial participation BOSTON-(BUSINESS WIRE)-The Institute for Healthcare Improvement (IHI), in partnership with Bristol Myers Squibb (BMS), is launching a new Cancer Collective Action Collaborative. This three-year effort will mobilize healthcare and community partners to drive meaningful, sustainable change in access to and participation in oncology clinical trials, with a particular emphasis on lung and breast cancer. "Removing barriers to clinical trials is both an imperative and an opportunity within our reach," said Shannon Stephens, MPH, IHI's Interim Vice President of Health Equity. "By valuing the lived expertise of patients alongside the clinical expertise of providers and taking a coordinated, collaborative approach, we can advance more equitable care and create sustainable change across the cancer care ecosystem." Building on the foundation established by the Rise to Health Coalition, the Collaborative will bring together 24 teams across the healthcare ecosystem to address clinical trial participation barriers among populations disproportionately affected by cancer. Through shared learning and coordinated action, teams will improve how health systems connect eligible patients to clinical trial opportunities; build reliable and inclusive pathways; strengthen patient and community engagement and trust; equip care teams and community partners; and leverage data to support continuous learning and improvement. "At BMS, we believe that every person should have the opportunity to benefit from our medicines and innovation, no matter who they are, where they live, or what they have," said Andrew Whitehead, Vice President, Head of Population Health at BMS. "The Cancer Collective Action Collaborative is an extension of our Population Health strategy, which shapes how we work to ensure access to care, including clinical trials that reflect the populations affected by disease." The challenge: advancing access and participation in oncology clinical trials. Cancer outcomes remain unequal across the United States. Black women are 38 percent more likely to die from breast cancer than White women, despite slightly lower incidence rates. Lung cancer mortality remains 14 percent higher among Black men than White men. Rural residents have significantly higher cancer incidence and mortality, such as 40 percent higher lung cancer risk, due to limited access to oncologists, fewer screening services, and longer travel distances for treatment. Patients also face unequal opportunities to participate in clinical trials. Approximately 80 percent of patients with cancer receive care from community oncologists, yet participation in clinical research remains uneven across care settings. Research has found that just 4.1 percent of patients at community cancer programs enroll in cancer treatment trials, compared with 21.6 percent at National Cancer Institute-designated comprehensive cancer centers. Racial, ethnic, and geographic differences in clinical trial participation further underscore the importance of addressing barriers associated with trial availability, recruitment processes, access to information, distance, and coordination across healthcare systems. "We cannot expect different outcomes if we continue to rely on the same approaches to clinical trial recruitment," said Dr. Megan Wanzo, Director of Global Patient Inclusion and Recruitment at BMS, who is leading the company's work on the Cancer Collective Action Collaborative. "Improving participation in oncology research requires us to examine how we make trials accessible, how we engage with communities, and how we equip health systems to connect patients to research opportunities. The opportunity before us is to move beyond identifying barriers to collectively changing the systems that sustain them." Through an in-person and virtual learning community, the Collaborative will bring together the following stakeholders to align efforts toward the Quintuple Aim for cancer care: - Health and healthcare organizations - Oncology practices - Community cancer centers - Community-based organizations - Patient advocacy organizations - People with lived experience Apply to join the Collaborative. IHI and BMS have completed the first phase of the initiative, co-designing the Collaborative using evidence-based improvement strategies to support effective collective action. With this foundation in place, IHI and BMS invite organizations to apply to join the Collaborative by November 30, 2026. Review the application details and apply here: https://go.ihi.org/4jyf3jT. For questions, contact [email protected]. About the Institute for Healthcare Improvement (IHI). The Institute for Healthcare Improvement (IHI) is a leading, globally recognized not-for-profit healthcare improvement organization that has been applying evidence-based quality improvement methods to meet current and future healthcare challenges for more than 30 years. IHI provides millions of people in healthcare with methods, tools, and resources to make care better, safer, and more equitable; convenes experts to enable knowledge sharing and peer-learning; and advises health systems and hospitals of all sizes in improving their systems and outcomes at scale. IHI's mission is to innovate and lead transformational improvement in health and healthcare worldwide. PRESS CONTACT: candice perodeau [email protected] 617-575-7723. Frequently asked questions. What is the purpose of the Cancer Collective Action Collaborative? The initiative aims to improve access to oncology clinical trials and address participation barriers. Who are the partners in this initiative? The initiative is a collaboration between the Institute for Healthcare Improvement and Bristol Myers Squibb. What cancers are primarily focused on in this initiative? The initiative focuses on lung and breast cancer. How can organizations join the Collaborative? Organizations can apply to join the Collaborative by November 30, 2026.

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).