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The Oncology Thematic Research Center at BMS is a key research and early development engine, responsible for the discovery and development of novel oncology therapeutics for patients. Centered at our state‑of‑the‑art research sites in Cambridge and Seattle, scientists focus on novel targets and pathways for tumors that are refractory to current therapies. With a deep understanding of the causal human biology, we are able to leverage our multiple modality platforms to best match the modality to the mechanism and desired outcome. We are a fully integrated drug discovery through translational and early clinical development organization which exploits state‑of‑the‑art in vitro, in vivo and ex‑vivo models of Cancer biology and Immuno‑oncology to identify and validate targets. We partner closely with colleagues in Translational Medicine, Informatics and Predictive Sciences and Early Clinical Development to generate biomarker and patient enrichment hypotheses to enable efficient decision making in early clinical trials. We are optimally positioned to complement the world‑class translational expertise, biology and leading academic research centers in the area. Position Summary We are seeking an experienced immunologist with clinical translational experience to join the Translational Research team within the Oncology Thematic Research Center at Bristol Myers Squibb in Cambridge, MA. The qualified candidate is a highly motivated, engaged, and creative scientist that can thrive in a highly matrixed organization to advance programs from candidate optimization through IND enabling activities and ultimately to Proof‑of‑Concept clinical trials. This individual will play a pivotal role in shaping and driving translational strategies for oncology assets, enabling the development of transformative cancer therapies for patients. Position Responsibilities Serve as a key scientific stakeholder in early clinical trial programs. Design and develop biomarker, pharmacodynamic, and target engagement assays to understand drug mechanism of action and response. Interact with project teams and contract laboratories for the design, execution, and oversight of molecular, cellular, and/or in‑vivo studies. Collaborate with cross‑functional teams and external partners (CROs, specialty labs) to generate high‑quality biomarker data for clinical studies. Contribute to translational plans, sample collection strategies, and documentation for early‑phase trials. Present experimental results and share scientific insights with project teams and stakeholders. Provide insight into novel ways to incorporate biomarkers into clinical designs to enable early understanding of emerging drug profiles, as well as input around tumor types and potential impact of biomarkers on internal decision making. Provide oversight to progress validated biomarkers into development of diagnostic assays, as needed. Participate in strategic review and input to presentations, publications and internal/ external communications along with accountable program leadership and in governance forums. Develop solutions and courses of action for senior staff, including identification of risks and risk mitigations. Share expertise, experience, lessons learned and knowledge with translational and other relevant scientific experts and colleagues across the organization. Basic Qualifications Bachelor's Degree 8+ years of academic and/or industry experience Or Master's Degree 6+ years of academic and/or industry experience Or Ph.D. or equivalent advanced degree in the Life Sciences 4+ of academic and/or industry experience Preferred Qualifications PhD and 6+ years of industry experience in drug development, ideally with at least 3 years in clinical translational research or translational medicine. Strong immunology experience, with an emphasis on solid tumor biology preferred. Experience in oncology translational biomarker roles, with solid tumor and immune‑oncology expertise strongly preferred. Strong scientific acumen and mechanistic understanding of disease biology, with demonstrated contributions to oncology and immuno‑oncology drug development. Hands‑on experience designing, executing, and analyzing translational biomarker assays and data across multiple technologies (e.g., genomics, immunohistochemistry, flow cytometry, immunoassays) and sample types in clinical studies. Familiarity with the drug development process and experience collaborating with clinical teams; able to communicate results and contribute to discussions in cross‑functional settings. Demonstrated ability to work effectively with internal stakeholders and external partners (e.g., CROs, specialty labs). Excellent communication, organizational, and teamwork skills, with a proactive and collaborative mindset. Eagerness to learn, grow, and take on increasing responsibility in a fast‑paced environment. Compensation Overview Cambridge Crossing: $159,290 - $193,022 The starting compensation range(s) for this role are listed above for a full‑time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job‑related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit Benefit Offerings Health Coverage: Medical, pharmacy, dental and vision care. Well‑being Support: Programs such as BMS Well‑Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP). Financial Well‑being and Protection: 401(k) plan, short‑ and long‑term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. Work‑life benefits include: Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)) Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non‑Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. All global employees full and part‑time who are actively employed and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. Equal Opportunity Employer Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law. #J-18808-Ljbffr