Bristol Myers Squibb

Recruitment

• Act as a strategic partner to hiring managers, aligning recruitment with organizational goals and metrics
• Anticipate talent needs, adapt to market changes, and influence hiring decisions
• Develop innovative recruitment strategies using industry trends and tools
• Collaborate with cross-functional teams to build effective talent pipelines
• Communicate BMS's commitment to science, innovation, and patient care
• Partner with Total Rewards to understand compensation structures and develop tailored offers
• Partner with branding, marketing, and talent sourcing teams to implement recruitment strategies and enhance the employer brand
• Align recruitment efforts with HR and business leaders' goals and workforce planning strategies
• Use AI tools and data analytics to improve recruiting strategies
• Analyze ATS and Tableau data to plan workforce needs, predict talent requirements, and improve hiring outcomes
• Implement AI solutions such as Eightfold and Paradox
• Build trust and inclusion through candidate interactions
• Develop meaningful relationships with candidates and stakeholders
• Enhance digital skills, data literacy, and sourcing capabilities across the workforce

Senior Talent Acquisition Partner – Agile

Supply Chain

• Lead the global strategy, governance, and execution oversight of Launch Excellence capabilities across the Cell Therapy portfolio
• Define and advance the long-term launch excellence roadmap
• Align Product Development, Operations, Supply Chain, Regulatory, Quality, and Commercial organizations for product launches and lifecycle changes
• Serve as the central integration point across development, manufacturing, supply chain, and commercial organizations
• Lead launch readiness, portfolio prioritization, resource alignment, risk management, and execution excellence
• Lead a team of Launch Excellence Managers and Professionals
• Establish operating models, governance, and digital capabilities for portfolio growth
• Drive responsible AI adoption and digital innovation in launch planning, forecasting, risk management, and execution
• Provide strategic oversight for Cell Therapy launch and lifecycle management programs
• Oversee launch scenario planning, portfolio sequencing, resource planning, risk mitigation, forecasting, and supply readiness assessments
• Establish processes to identify emerging risks, capacity constraints, and execution challenges
• Monitor post-launch performance and capture lessons learned
• Develop and operationalize a Product Obsolescence Process & Execution Framework
• Define obsolescence governance, decision rights, stage gates, escalation pathways, and execution playbooks
• Coordinate inventory disposition, regulatory and quality dependencies, commercial alignment, and stakeholder communications
• Partner cross-functionally to identify obsolescence triggers, assess patient and business impact, and coordinate mitigation plans
• Create standardized tools, templates, metrics, and executive reporting mechanisms
• Interface with Cell Therapy Operations, Development, Supply Chain, Commercial, Regulatory, Quality, and Finance organizations
• Align global and regional leadership teams on priorities, tradeoffs, timelines, and risk management
• Influence enterprise decisions through executive-level communication and strategic recommendations
• Partner with Commercial organizations to align market demand strategies and supply readiness plans
• Collaborate with manufacturing sites, product leaders, supply planning, regulatory, and quality organizations
• Build and lead a high-performing Launch Excellence organization
• Define future-state operating models, capabilities, tools, systems, and governance frameworks
• Establish standards, playbooks, methodologies, training programs, and best practices
• Develop talent pipelines and succession plans

Senior Director, Launch & Lifecycle Management Excellence, Cell Therapy Supply Chain

Therapist

• Lead worldwide Medical Affairs strategy for arlo-cel, a GPRC5D CAR T in clinical development for multiple myeloma
• Drive global launch readiness across external communications, market shaping, and internal readiness
• Lead cross-functional arlo-cel initiatives and integrate strategies across the multiple myeloma portfolio
• Collaborate with local Medical Affairs teams to align global launch strategies and market-ready action plans
• Drive cross-asset collaboration and knowledge sharing across Cell Therapy and Oncology
• Establish relationships with thought leaders and KOLs at academic centers, cooperative groups, steering committees, and advisory boards
• Provide strategic input to publication planning, abstracts, presentations, and publications
• Develop and implement congress strategies for COMy, EHA, IMS, and other major meetings
• Provide input into sponsored symposia and independent medical education events
• Refine the Integrated Evidence Plan and provide input on evidence generation, ISR and CRC trials, and HEOR analyses
• Represent arlo-cel on the WW MM Asset Indication Medical Strategy team
• Review publications and update launchpad assets, slide decks, training sessions, and Q&A materials
• Provide medical insights for clinical development plans and strategic decision-making
• Serve as a subject matter expert to cross-functional multiple myeloma partners
• Collaborate with market access, marketing, and patient advocacy teams

Senior Director, Cell Therapy – Multiple Myeloma

Procurement

• Design and execute proactive executive talent sourcing strategies by mapping target companies, talent pools, and diverse leadership communities
• Identify, engage, and cultivate long-term relationships with passive executive talent through personalized outreach, networking, and thought-leadership engagement
• Build and maintain robust candidate pipelines for current searches and succession planning
• Conduct deep market research and competitive intelligence on talent availability, compensation benchmarks, and competitor organizational structures
• Partner with recruiters and hiring leaders as a consultative advisor, calibrating strategy and presenting qualified, diverse candidate slates
• Develop future candidate pipelines and talent maps, determining the optimal job advertising mix
• Aggregate market and industry data to support compensation negotiations and strategic recruiting methods
• Develop and maintain relationships with recruitment agencies, educational institutions, professional associations, and industry networks
• Ensure compliance with labor laws, regulations, industry standards, equal employment opportunity, diversity, and labor relations requirements
• Serve as a Bristol Myers Squibb brand ambassador and build trusted relationships with senior leaders and candidates
• Ensure exceptional candidate and stakeholder experiences while maintaining compliant recruiting and hiring practices
• Participate in industry forums, elevate BMS’s employer reputation, and bring insights into the organization for continuous improvement
• Partner with Total Rewards, Global Mobility, Legal, Immigration, and Procurement on executive offer development, negotiation, and delivery
• Collaborate with non-executive recruiting teams to ensure transparency, talent sharing, and continuity across sourcing and recruiting efforts

Executive Talent Sourcing & Pipelining Lead, Associate Director

General

• Promote approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets compliantly
• Create demand for BMS medicines by presenting balanced clinical and scientific rationale to healthcare providers
• Maintain and grow scientific expertise in assigned products and therapeutic areas
• Prepare and implement comprehensive territory and account plans
• Use CE^3 and other available tools to derive insights and inform call plans
• Conduct in-office presentations and discuss label-consistent product-related scientific information with healthcare providers
• Organize external speaker programs, including approved speaker selection, scheduling, and logistics
• Maintain working expertise on emerging data for approved indications
• Engage Medical on Call for unsolicited questions and complex technical inquiries
• Collaborate with other field teams to deliver the best customer experience
• Gather and share customer insights internally with appropriate stakeholders
• Comply with all laws, regulations, and BMS policies

Senior Therapeutic Area Specialist, Oncology

Clinical Specialist

• Build and sustain strategic relationships with KOLs and institutional stakeholders across nuclear medicine, radiology, radiation oncology, radiation safety, health physics, nursing, and advanced practice
• Lead site readiness and workflow integration for approved agents and clinical trials
• Address product handling, administration, radiation safety, and radiopharmaceutical licensing considerations
• Deliver clinical and technical education for safe, effective, and guideline-aligned product utilization
• Serve as a senior subject matter expert in nuclear medicine and radiopharmaceutical applications
• Maintain expertise in imaging techniques, oncology practice patterns, and emerging therapeutic advances
• Support clinical trial execution through site training and protocol education
• Respond to unsolicited scientific inquiries while ensuring documentation and regulatory compliance
• Generate field insights on diagnostic imaging and radiopharmaceutical trends, institutional barriers, and adoption dynamics
• Inform launch strategy with actionable field insights
• Provide medical and scientific congress support as requested
• Ensure adherence to SOPs and regulatory frameworks, including the U.S. Compliance Code of Conduct, OIG Guidance, PhRMA Code, GCP, HIPAA, and applicable FDA regulations
• Apply AI to improve team execution and decision-making

Clinical Theranostic Specialist

Cloud Engineer

• Serve as the technical owner and primary builder of the AWS Landing Zone architecture using Control Tower, AWS Organizations, and Transit Gateway
• Author and maintain enterprise-grade Infrastructure-as-Code modules using CloudFormation and GitHub under a strict GitOps model
• Architect, design, and validate scalable, resilient, cost-efficient cloud-native enterprise application architectures
• Design applications for disaster recovery in an IaaS cloud platform
• Build robust, scalable, secure cloud-native solutions using CloudFront, Lambda, API Gateway, Elastic Beanstalk, ECS, DynamoDB, and S3
• Embed security automation throughout CI/CD pipelines using policy-as-code and automated compliance checks
• Define and implement standards for AWS Config, IAM roles and policies, and organization policies
• Own the cloud platform and developer toolchain as internal products, improving developer experience and time to market
• Lead integration of generative AI, intelligent testing, and automated security patch recommendations into the SDLC
• Architect and optimize the enterprise CI/CD platform using GitHub Actions or equivalent tooling
• Develop automated mechanisms and reference architectures to optimize AWS spend and resource utilization
• Establish technical standards, design patterns, and quality gates for cloud adoption and regulatory compliance
• Lead technical reviews for major cloud projects
• Mentor teams and provide authoritative technical leadership

Associate Director, Lead Cloud Architect

Director

• Own the technology roadmap and lifecycle for Automated QC equipment and software, including upgrades, vendor management, and long-term platform planning
• Lead deployment of Automated QC systems at new and existing nodes across the Cell Therapy manufacturing network
• Sequence and coordinate priorities across concurrent programs
• Partner with Assay and Data Automation and Analytical Sciences and Technology to define system requirements, validate performance, and resolve technical issues
• Serve as primary point of contact for receiving sites and ensure operational and quality readiness before go-live
• Represent Automated QC strategy and progress in network-level technical and governance forums
• Identify deployment timeline and system performance risks and drive mitigation plans
• Ensure Automated QC systems and processes meet cGMP requirements
• Support regulatory filings as needed
• Establish key performance metrics and report deployment progress to stakeholders and leadership
• Lead, coach, and develop the team supporting deployment and sustaining operations

Director, QC Automation

• Represent WW Medical Affairs as therapeutic area expert and provide scientific leadership and support for CAR T compounds in various stages of clinical development
• Lead cross-functional initiatives for Multiple Myeloma and Solid Tumor pipeline assets
• Align disease strategy and tactics with local medical affairs teams
• Develop strategic plans for cell therapy entry into Solid Tumor and provide medical input to early asset portfolio strategy
• Drive cross-asset collaboration and knowledge sharing across Cell Therapy and Oncology
• Establish and cultivate relationships with thought leaders
• Guide publication planning and execution; review abstracts, presentations, and publications
• Develop and implement congress strategies and organize BMS-sponsored symposia
• Refine the Integrated Evidence Plan (IEP)
• Review publications and update launchpad assets, slide decks, training sessions, and Q&A materials
• Lead and support global advisory boards and strategic committee meetings
• Assist regional teams with globally impactful advisory initiatives
• Provide medical perspective on evidence generation, ISR and CRC trials, and HEOR analyses
• Ensure scientific excellence in medical education and effective data exchange
• Provide medical insights for clinical development plans and strategic decision-making
• Serve as subject matter expert for Multiple Myeloma asset and portfolio decisions and Solid Tumor early-asset strategy
• Collaborate with global and local market access and marketing teams
• Work with patient advocacy to align objectives and enhance engagement
• Travel approximately 15–20% in the US and globally

Director, Cell Therapy – Multiple Myeloma and Solid Tumor Pipeline

• Promote approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets compliantly
• Create demand for BMS medicines by presenting balanced clinical and scientific rationale for use in appropriate patients
• Maintain and grow scientific expertise in assigned products and therapeutic areas
• Prepare and implement comprehensive territory and account plans
• Use SOPHIA and other tools to derive insights and inform call plans
• Present approved scientific resources and publications accurately to healthcare providers
• Conduct in-office presentations and discuss product-related scientific information consistent with product labeling
• Organize external speaker programs, including speaker selection, scheduling, and logistics
• Maintain working expertise on emerging data for approved indications
• Engage Medical on Call for unsolicited questions and complex technical inquiries
• Collaborate with other field teams to provide the best customer experience
• Gather and share relevant customer insights internally
• Comply with all laws, regulations, and BMS policies
• Travel in the field to visit external customers and attend meetings as directed

Senior Therapeutic Area Specialist, Cardiovascular Specialty

• Partner with Pharmacology, DMPK, Toxicology, and Translational Science leaders to shape and deliver the technology roadmap for non-clinical decisions
• Lead deployment of GenAI, agentic, and predictive AI/ML capabilities for non-clinical workflows
• Advance predictive safety, in silico DMPK, histopathology image AI, and study design support
• Ensure high-fidelity capture of non-clinical data in source systems and clean downstream flow to the R&D Data organization
• Support animal welfare data, IACUC-related processes, and study-governance workflows
• Enable non-clinical safety signal detection and risk characterization through analytics and decision-support tools
• Partner with Development teams to feed clinical findings into non-clinical model validation and refinement
• Ensure operational excellence and reliability of non-clinical applications, modeling environments, and analytics
• Lead and develop a team of scientific technologists, AI/ML engineers, product leaders, and application specialists
• Translate scientific needs into scalable, integrated technology solutions for Research

Senior Director, In-Vivo & Non-Clinical Pharmacology

Artificial Intelligence

• Develop, implement, and optimize end-to-end machine learning pipelines for clinical study design and execution
• Automate workflows processing and analyzing clinical trial protocols, real-world evidence, and patient recruitment data
• Ensure scalability, reliability, and robustness of machine learning solutions for real-time decision support
• Partner with IT, medical, development, and biostatistics teams to co-develop AI-driven solutions
• Liaise between technical teams and non-technical stakeholders
• Translate technical insights and model results into actionable strategies for clinical operations teams
• Oversee AI product lifecycles from ideation and development through deployment and monitoring
• Develop and execute project plans aligned with clinical development timelines
• Conduct post-deployment analysis and identify opportunities for continuous improvement
• Evaluate emerging data science and AI trends and integrate NLP and predictive analytics into clinical trial workflows

Senior Manager, Analytical AI Clinical Development

• Define and execute the strategic vision for the AMS Separations organization
• Build organizational capability through talent development, succession planning, workforce planning, performance management, and strategic hiring
• Develop future technical and people leaders and create a sustainable pipeline of scientific talent
• Establish priorities and allocate resources across multiple products, platforms, and business initiatives
• Drive organizational effectiveness, flexibility, simplification, and continuous improvement
• Foster accountability, collaboration, technical excellence, and innovation
• Provide strategic oversight and scientific direction for analytical lifecycle management, validation, transfer, comparability, remediation, and method performance monitoring
• Serve as the technical escalation point for complex scientific issues, analytical risks, and business-critical decisions
• Guide technical strategy and development of capabilities for evolving portfolio needs
• Coach and develop scientists in technical decision-making, problem-solving, and scientific leadership
• Partner with Quality Control, Analytical Development, MS&T, Regulatory, Manufacturing, and Product Teams
• Drive alignment between commercial needs, analytical capabilities, and resource planning
• Support regulatory submissions, inspections, audits, and health authority interactions
• Contribute to analytical CMC strategy and dossier authorship for licensure
• Contribute technical expertise to responses to Health Authority queries
• Drive organizational effectiveness, operational excellence, talent development, and strategic execution as a member of the AMS leadership team

Associate Director – Separations, Analytical Method Sciences

Medical Director

• Provide data management leadership, insight, and support to internal and external projects and clinical trials
• Serve as lead Clinical Data Manager for multiple clinical trials when needed
• Ensure collected data meets study objectives and company quality standards
• Manage and oversee data management personnel and CRO/vendor activities
• Ensure CRO adherence to project timelines from study startup through closeout
• Participate in cross-functional meetings and provide project status, issue, and milestone updates
• Review data using listings and visualization tools for performance and quality reporting
• Conduct within-study and cross-study trend analyses
• Lead third-party vendor interactions regarding collection, transmittal, and transfer of study-specific data
• Contribute to SOP development and updates for regulatory compliance and operational needs
• Travel approximately 10%

Associate Director, Clinical Data Management

• Serve as the Clinical Data Management program lead for a new product and lead individual studies from study start-up through database lock
• Develop and drive data management strategy, including study start-up planning, database build oversight, data review, risk management, database lock, and submission readiness
• Lead program- and study-level data management execution to deliver high-quality, timely, decision-ready clinical trial data
• Oversee CROs and data management vendors, ensuring accountability, quality, compliance, and adherence to timelines
• Partner with Biostatistics, Statistical Programming, Clinical Operations, Medical Monitoring, Safety, Regulatory Affairs, and other stakeholders
• Lead cross-functional data reviews and identify, escalate, and resolve data issues, trends, risks, and quality concerns
• Oversee or contribute to Data Management Plans, edit check specifications, validation plans, reconciliation plans, data transfer agreements, data review plans, and database lock documentation
• Leverage AI to drive program, portfolio, or functional performance through prioritization and scaled adoption
• Travel approximately 10% of the time; evening and weekend work may be required