Bristol Myers Squibb

Director

• Support clinical development of RayzeBio radiopharmaceuticals for oncology indications
• Collaborate with clinical development on ongoing clinical trial program activities
• Support functional area activities during program implementation and clinical study start-up, execution, and close-out
• Contribute to data analysis and reporting and potentially support NDA/MAA filings
• Develop or oversee development of study concept synopses and protocols
• Participate in protocol review discussions on scientific and procedural aspects of study design
• Prepare study protocols, amendments, study manual sections, Investigator meeting materials, and other documents with guidance and supervision
• Contribute to the design, development, and review of CRFs, Data Management Manuals, and Data Analysis Plans
• Review ongoing clinical data
• Organize and oversee Data Review Committee meetings and prepare slides and meeting materials
• Address Investigator questions regarding scientific and procedural issues with MD supervision
• Prepare or review data listings, summary tables, study results, manuscripts, and scientific presentations
• Assist with INDs, regulatory documents, IND annual reports/DSURs, Investigator Brochures, and NDAs/MAAs
• Support functional-area priorities and implement solutions to moderately complex clinical-study obstacles
• Coordinate teams and provide direction as needed
• Lead two or more components of departmental strategic initiatives as needed
• Advise colleagues on decisions and resolution of moderately complex problems
• Leverage AI tools to enhance productivity and work quality

Associate Director of Clinical Science

• Serve as BMS's subject-matter expert and strategic lead for LCAs and PCFs
• Build, run, and critically review audit-ready, third-party-verifiable cradle-to-gate and cradle-to-grave LCAs/PCFs for BMS products
• Develop the PCF/LCA multi-year strategy and advise where the company invests
• Build the internal operating model, including governance, standard methodologies, digital tools, data-management systems, training, and tools for non-specialists
• Own PCF/LCA technology implementation and lifecycle, including guiding the Watershed platform's tool design, data quality, and fit to business and regulatory needs
• Translate external product-stewardship regulations and mandates into executable internal programs and repeatable workflows
• Represent BMS in industry workstreams and projects
• Embed life cycle thinking into design, formulation, packaging, device, and sourcing decisions
• Build a roadmap for how LCA/PCF informs product development and procurement decisions
• Engage suppliers and external standards bodies
• Help operationalize other Product Stewardship regulations across the business
• Participate in global research projects, environmental support of sites, extended producer responsibility, chemical registrations, and hazard communication as time permits
• Act as primary backup for the Product Stewardship Lead

Director, Life Cycle Assessment – Product Stewardship

Therapist

• Oversee management of multiple development and life-cycle management projects of varying priorities and complexities
• Represent GRS-CMC on cross-functional teams, governance committees, and due diligence/in-licensing projects
• Represent BMS at Health Authority meetings
• Serve as a credible spokesperson with key stakeholders and Health Authorities
• Develop and communicate strategic direction based on global regulatory guidelines and experience
• Seek opportunities for external regulatory engagement for themselves and/or team members
• Prepare or oversee preparation of CMC submissions, ensuring thoroughness, completeness, and timeliness
• Review CMC Lead submissions for clarity of strategic and technical content
• Utilize electronic systems for dossier creation, review, and tracking
• Manage and actively support the growth and development of direct reports
• Participate in leadership and department meetings
• Anticipate and communicate possible regulatory paradigm shifts
• Participate in product fact-finding meetings and R&D forums representing GRS-CMC
• Support preparation of CMC policies and procedures
• Maintain oversight and promote regulatory compliance through timely and accurate data entry into the Regulatory Information Management system

Director, Regulatory CMC – Cell Therapy

Medical Science Liaison

• Identify disease- and product-related medical needs in a defined geography
• Develop and maintain relationships with thought leaders and healthcare providers
• Engage in peer-to-peer scientific exchange to support medical education, data generation, insight generation, and patient access
• Serve as a medical resource for external stakeholders
• Identify, develop, and enhance relationships with research thought leaders, HCPs, and access stakeholders
• Use 1:1, group presentation, remote, and other interaction channels
• Assess the medical landscape and understand stakeholder needs and expertise
• Maintain knowledge of treatment strategies, products, unmet medical needs, clinical trials, and scientific activities
• Understand the competitive landscape and address customer informational needs
• Partner with HCPs on disease-state initiatives, collaborative research, company-sponsored trials, and investigator-sponsored research
• Attend and provide scientific support at medical congresses and local/regional meetings
• Collect and communicate meaningful medical insights to medical organizations to support strategy development
• Support clinical trials to enhance patient recruitment, enrollment, and discussions around safe and effective use of investigational products
• Provide recommendations and insights to clinical development teams on study and site feasibility
• Act as primary liaison to investigators interested in developing, submitting, and performing investigator-sponsored research
• Spend the majority of time in the field with the team and external customers

Medical Science Liaison, Hematology – Myeloid

General

• Promote approved indications of BMS products within a defined territory to meet or exceed assigned sales targets compliantly
• Drive demand for BMS medicines for appropriate patients
• Engage healthcare providers through differentiated customer experiences and scientific dialogue consistent with product labeling
• Build and maintain professional credibility with regional thought leaders, community physicians, HCPs, office staff and other patient-care stakeholders
• Liaise with other BMS functions to deliver a higher customer experience
• Prioritize safe and appropriate use of BMS products while achieving business results and performance objectives
• Spend 100% of time in the field with external customers
• Maintain and grow scientific expertise in assigned products and therapeutic areas
• Prepare and implement comprehensive territory and account plans
• Use CE^3 and other tools to derive insights and inform call plans
• Present approved scientific information to HCPs in office presentations and lunch-and-learns
• Organize external speaker programs, including speaker selection, scheduling and logistics
• Maintain working expertise on emerging data for approved indications
• Use Medical on Call for unsolicited questions and complex technical inquiries
• Collaborate with field teams and share customer insights internally
• Comply with laws, regulations and BMS policies

Senior Therapeutic Area Specialist

• Drive demand for BMS medicines within the assigned oncology portfolio for appropriate patients
• Engage healthcare providers through differentiated customer experiences and scientific dialogue consistent with product labeling
• Build and maintain credibility with regional thought leaders, community physicians, HCPs, office staff, and patient-care stakeholders
• Liaise with other BMS functions to deliver a higher customer experience
• Promote approved indications of BMS products within the assigned territory and meet or exceed sales targets compliantly
• Articulate the clinical and scientific rationale for product use in appropriate patients
• Maintain and grow scientific expertise in assigned products and therapeutic areas
• Prepare and implement comprehensive territory and account plans
• Use CE^3 to derive insights and dynamically inform call plans
• Conduct in-office presentations and discuss product-related scientific information with HCPs
• Organize external speaker programs, including speaker selection, scheduling, and logistics
• Maintain working expertise on emerging data for approved indications
• Use Medical on Call to answer unsolicited questions and complex technical inquiries
• Collaborate with other field teams
• Gather and share customer insights internally
• Comply with applicable laws, regulations, and BMS policies
• Spend 100% of time in the field with external customers

Senior Therapeutic Area Specialist, Oncology

Lead Generation

• Define and drive the integrated evidence generation strategy aligned with Medical Affairs and overall product strategy
• Lead evidence generation across Phase II/IV clinical trials, real-world evidence, non-interventional studies, registries, observational research, and health outcomes studies
• Critically assess research concept designs for strategic alignment with BMS priorities and stated objectives
• Lead or significantly contribute to protocol development, including study design, objectives and endpoints, eligibility criteria, statistical considerations, and operational feasibility
• Engage in peer-to-peer scientific dialogue with external research partners to optimize study design elements
• Deliver studies from concept ideation through governance approval and throughout the study lifecycle
• Serve as a thought leader on evidence generation methodologies
• Lead preparation and delivery of evidence generation proposals, updates, and results to governance bodies and cross-functional stakeholders
• Apply GCP, ICH guidelines, and clinical trial governance knowledge to ensure compliant, high-quality study execution
• Partner with Clinical Operations and CROs to deliver studies on time, on budget, and with high data quality
• Participate in advisory boards, steering committees, and scientific forums
• Collaborate across functions, geographies, and therapeutic areas for cohesive evidence generation planning and execution
• Oversee operational delivery, scientific rigor, quality, compliance, timelines, and budgets
• Contribute to publications, abstracts, congress presentations, and advisory boards

Director, Global Medical Evidence Generation Lead, Oncology

AI Engineer

• Develop, test, maintain, and enhance software applications and components using modern programming languages
• Write clean, secure, maintainable, and efficient code following software development standards and best practices
• Collaborate with engineers, product owners, and business users to understand requirements and translate them into technical solutions
• Troubleshoot, debug, and resolve application issues, escalating risks or complex problems when needed
• Participate in code reviews and contribute to code quality, testing, and development practice improvements
• Support application integration with APIs, databases, cloud services, and software tools
• Use AI-assisted development tools or AI agents for coding, testing, debugging, and documentation
• Contribute to continuous improvement of development processes, agile engineering practices, and secure application development

Software Engineer, AI Engineering, Enablement

• Serve as a core member of the Global Medical Sotyktu and Sjögren’s Disease Launch Teams
• Lead global Sjögren’s Disease medical affairs and develop direct reports within the Rheumatology medical team
• Develop, communicate, and execute the global medical strategy and tactical plan for Sjögren’s Disease
• Request and manage the medical budget to execute the global strategy
• Represent Medical Affairs in cross-functional leadership forums and align with clinical, market access, and commercial teams
• Provide expert opinion on pathophysiology, diagnosis, and unmet medical needs
• Partner with the medical matrix team on global medical strategy, launch plans, evidence generation, and medical communications
• Build relationships with core market medical teams, global key opinion leaders, and professional societies
• Lead advisory meetings and Phase 3 program data analysis
• Collaborate on real-world studies
• Translate evidence into publications and maintain scientific resources with Medical Communications
• Maintain engagement with key opinion leaders and Sjögren’s Disease program collaborators
• Report to the Senior Director, Global Sotyktu Medical Product Lead

Director, Global Medical Affairs – Sjogren’s Disease

• Engage in peer-to-peer scientific dialogue with regional, national, and healthcare professional thought leaders within a defined geography
• Engage top HCPs in high-disease-burden hospitals
• Translate scientific evidence into patient care
• Capture medical insights and advise cross-functional partners as a clinical and scientific advisor
• Ensure interactions align with enterprise and medical strategies and support patient access to BMS medicines
• Address scientific questions beyond approved assets and indications
• Conduct pre-launch, peri-launch, and lifecycle medical engagement
• Deliver educational dialogue and share clinical evidence according to physician needs and the field medical plan
• Serve on a scheduled basis as Medical on Call, answering unsolicited off-label and technically complex questions virtually
• Spend the majority of time in the field interacting with investigators, clinical thought leaders, and other external stakeholders
• Develop trusted relationships with academic and community neurology thought leaders through proactive and reactive interactions
• Collaborate with thought leaders to gather clinical-landscape insights and develop product- and disease-focused medical plans
• Engage medical societies, patient advocacy groups, and guideline committee members
• Train external speakers as needed
• Engage payers during pre- and peri-launch phases with fHEOR and Account Executives
• Document and achieve annual goals
• Leverage digital capabilities to enhance medical engagement
• Advise clinical development teams on study and site feasibility
• Liaise with large accounts regarding clinical barriers and equitable access to trials
• Lead major evidence read-outs with clinical trial investigators
• Support interventional and non-interventional research studies, including identifying and assessing study sites
• Support HCPs through ISR submission, execution, and follow-up
• Ensure investigators understand and apply BMS pharmacovigilance procedures and alert personnel to adverse events
• Support CRO-sponsored studies as agreed with home office medical and GDO

Medical Science Liaison, Neurodegeneration

Research Scientist

• Apply bioinformatics, statistical, modeling, and computational biology approaches to analyze large-scale clinical datasets
• Drive translational insights across the BMS solid tumor oncology portfolio
• Analyze clinical and real-world patient datasets to discover biomarkers, elucidate disease biology, and inform pipeline development strategies
• Partner with biomarker scientists, clinical development teams, and preclinical researchers
• Design and execute computational strategies for clinical and translational studies
• Analyze high-dimensional molecular datasets to generate mechanistic insights into treatment response and resistance
• Apply and/or develop ML/AI methods for predictive modeling, feature selection, and multi-modal data integration
• Provide scientific leadership and mentorship
• Shape analytical best practices and elevate AI-enabled approaches across the team
• Communicate scientific results to R&D decision-making bodies
• Translate complex analyses into actionable recommendations influencing cross-functional strategy

Principal Scientist, Translational Informatics, Predictive Sciences

Community Manager

• Drive demand for BMS medicines within the cardiovascular portfolio for appropriate patients
• Engage healthcare providers through differentiated customer experiences and scientific dialogue consistent with product labeling
• Build and maintain professional credibility with regional thought leaders, community physicians, HCPs, medical groups, office staff, and patient-care stakeholders
• Liaise with other BMS functions to deliver a higher customer experience
• Prioritize safe and appropriate use of BMS products while meeting business and performance objectives
• Promote approved BMS product indications within a defined territory or region
• Articulate the clinical and scientific rationale for products in appropriate patients
• Maintain and grow scientific expertise in assigned products and therapeutic areas
• Prepare and implement territory and account plans
• Use SOPHIA to derive insights and inform call plans
• Provide tool feedback to leadership for continuous improvement
• Present approved scientific resources and publications to HCPs with medical accuracy
• Conduct in-office presentations such as lunch-and-learns
• Organize external speaker programs, including speaker selection, scheduling, and logistics
• Maintain working expertise on emerging data for approved indications
• Use Medical on Call for unsolicited questions and complex technical inquiries
• Collaborate with field teams to support HCP customer experience
• Gather and share customer insights internally
• Comply with laws, regulations, and BMS policies

Senior Therapeutic Area Specialist, Cardiovascular Community

• Implement RayzeBio’s vision for growth and lead efforts enabling digital processes for commercialization objectives
• Maintain and enable the digital systems roadmap for launch and commercialization of radiopharmaceutical technologies
• Operate and maintain digital solutions for commercial systems, including operations, planning, and ordering portals, plus associated infrastructure
• Deliver service-level management processes with IT groups and vendor-managed services, including SLAs, disaster recovery, and service continuity
• Align the digital roadmap with business outcomes and drive value realization
• Lead indirect reports and service providers in delivering effective, innovative, and stable solutions
• Partner with functional leaders to develop and align business-process improvement strategies through information-systems automation
• Provide IT leadership for regulatory inspection readiness and data-integrity initiatives
• Ensure risk-based validation for assigned functions
• Manage new demand and evolve digital solutions and mindset
• Identify technology trends and leverage innovative technologies to provide organizational solutions
• Participate in strategic communications with business and functional leadership teams
• Develop long-term three-year roadmaps identifying capabilities with the greatest business impact
• Set and manage budgets and collaborate with architectural, IT, and business partners
• Report directly to the Executive Director, IT

Associate Director, IT Commercial Systems

• Own global medical strategy for a subset of hematology and oncology early-development assets from candidate selection through clinical proof-of-concept
• Provide medical accountability for a set of early HO assets
• Manage cross-functional relationships across R&D, Medical, and Commercial teams
• Serve as a core member of early asset Global Program Teams
• Partner with Global Program Leads, Clinical Development leads, Translational Medicine leads, and HO Medical/Commercial teams to deliver program objectives and milestones
• Ensure development of differentiated early Target Product Profiles and contribute to early Clinical Development Plans
• Own early Integrated Evidence Plans to drive innovative data generation and accelerate and de-risk clinical development
• Own medical communications strategies and develop scientific narratives and publication strategies
• Engage external Thought Leaders and Patient Advocacy groups to inform compound strategies, asset decisions, and portfolio tradeoffs
• Lead planning and execution of advisory boards
• Work effectively in a highly matrixed environment with an enterprise mindset

Senior Director, Early Differentiation & Pipeline Strategy, Oncology

Manager

• Serve as the primary GTS lead for data and digital governance, compliance, data stewardship, and lifecycle obligations across the GTS digital portfolio
• Champion data governance practices covering data integrity, ownership, traceability, retention, and compliance
• Drive resolution of governance gaps, operational issues, compliance findings, and data quality concerns through coordination, escalation, and action tracking
• Monitor portfolio health, compliance status, lifecycle milestones, risks, and operational performance
• Provide visibility, insights, and recommendations to GTS leadership
• Partner with GTS business representatives, GTS BI&T Partners, Quality, Compliance, Procurement, and external providers
• Lead recurring governance activities, periodic reviews, documentation maintenance, training compliance, lifecycle assessments, vendor engagements, and audit readiness
• Improve data governance execution, data management practices, operational effectiveness, and adoption of standardized digital processes
• Assess emerging digital capabilities and support requirements for governance, lifecycle planning, alignment, and sustainability
• Drive alignment across GTS, BI&T, Quality, Compliance, and vendor organizations
• Lead planning, prioritization, and execution of critical governance and operational activities