Financial Planning and Analysis

• Ensure the company's financial matters are managed effectively and efficiently
• Ensure compliance, strong internal control environment and focus on working capital management
• Actively partner with business leaders to develop business strategy
• Identify business opportunities & prioritize investment and resources
• Provide strategic input in business development deals
• Collaborate with key internal and external stakeholders
• Partner with cross functional team to support preparations and planning for new products
• Drive innovation and productivity mindset in finance team
• Ensure efficient collaboration and process alignment with regional & shared service teams
• Lead and develop the GLE Finance team

Finance Director – Gulf, Libya, Egypt

Director

• Reporting directly to the Head of their assigned functional area and acting as a member of their Leadership Team
• Leads global geographic strategy and performance across assigned region / geography.
• Responsible for translating functional area and GDMS strategic imperatives into region-specific priorities and plans.
• Partners with GDMS and GCTO leaders to drive global alignment, standardization, and transformation of data-management practices
• Represents their function and geography network in GDMS LT forums, and ensure resource excellence, capability growth, and operational readiness worldwide.
• Oversee multiple regions/countries to ensure excellence in functional management and regulatory compliance.
• Collaborate with cross-functional (non-GDMS) leadership and enterprise support functions within assigned geographies to achieve strategic and operational goals and objectives.
• Embed process-excellence and governance frameworks across regions.
• Shape and implement digitally enabled operating models; drive global alignment, standardization, and transformation.
• Champion a culture of collaboration, innovation, and accountability across the network; ensure ongoing improvement and operational excellence.
• Partner with leaders across GDMS, GCTO, and Global Clinical Development (GCD) to drive consistent rollout / adoption of capabilities.
• Serve as escalation point for country/regional issues; oversee region-specific risk, escalation, and capacity-management processes; ensure local regulatory, business, and labor compliance.
• Drive adoption of leading-edge technology deployment principles across relevant GCTO organizations and functions.
• Lead complex cross-functional workstreams driving automation, data integrity, and operational excellence from idea/design through implementation and value realization.
• Lead recruiting and hiring and oversee performance management activities, including management of sensitive employee-relations matters in partnership with HR.

Executive Director, Clinical Data Management – Europe

Marketing

• Provide oversight into the development of access strategies for our New Products portfolio.
• Responsible for managing the early access planning for 10+ new oncology assets in our pipeline.
• Driving projects supporting list price, lifecycle gross to net and discount/contracting assumptions, IRA legislation and policy impacts.
• Collaborate with multiple stakeholders within our organization to ensure transparency and alignment to future access opportunities and challenges.
• Create and maintain early access strategies for each portfolio asset including: Input on evidence generation and evidence needs value messaging list price strategy contracting options across segments.
• Support of portfolio-based access strategies Finance alignment and management of access inputs to annual and long-term forecasting for new products.
• Capability building: creation and maintenance of modeling, research, dashboards and analysis supporting early product access.

Director, Oncology OCAR – New Product Payer Marketing

• Provide commercial leadership into asset development programs, working in close collaboration with cross-functional Product Development Teams and Asset Development Teams to create Target Product Profiles, conduct forecasting and contribute to tumor-area strategy
• Provide commercial leadership, where appropriate, into Scientific Strategy development & execution (e.g., Congress Planning, Scientific Platform development, Medical Education programs, Patient Engagement etc.) and collaborate with Medical / Health Economics and Outcomes Research (HEOR)
• Development of Global Brand Strategy and Campaign, including scientific narratives, positioning of assets within a disease area, key messaging, and as needed, content development leadership
• Collaboration across teams to develop, plan and support commercial and enterprise readiness for worldwide product launches and campaigns
• Collaboration with regions and key markets to develop global strategy for a tumor area, while supporting local needs
• Participate in the development of customer engagement strategy and scientific expert leader engagement
• Through detailed competition tracking and assessment, inform commercial planning assumptions, strategy and positioning
• Develop competitive response planning
• Provide commercial leadership, where appropriate, for the creation & implementation of internal/external communications for the disease/tumor area

Director, Global Oncology - GI Cancers

Research Scientist

• Support the strategic design, development, and delivery of efficient, flexible, and modular analysis and reporting and submission standards and tools that can be used for drug and/or vaccine projects across all therapeutic areas.
• Adheres to standard operating procedures and guidelines established by the department.
• Drives data structures that include analysis and reporting data standards and submission standards.
• Actively leads and contributes to the department's strategic initiatives.
• Key collaborator with internal and external stakeholders including Biostatistics, Statistical Programming, Data Management, Clinical Research, Regulatory, Observational Research, Clinical Safety, and PK/PD Modeling and Simulation organizations.
• Drive the development and adoption of scalable, reusable multilingual standards library based on R, Python and SAS with an emphasis on open-source adoption and automation, leveraging AI where appropriate.
• Address operational challenges that require strategic standard-based solutions, resulting in improved analysis and reporting deliverables.
• Facilitate global adoption of standards and programming best practices.
• Provide technical consultation and analytical support to statistical programmers and statisticians.
• Lead and actively contribute to departmental strategic initiative project teams.

Principal Scientist, Statistical Programming – A&R Standards, Innovation

Communications

• Develop and implement integrated communications activities in support of our company’s oncology in-line products and Phase 3 pipeline assets;
• Heavy emphasis on data milestone communications (data releases, medical meeting communications) and regulatory milestones and approvals.
• Drive integrated editorial strategy to raise external awareness of late-stage oncology pipeline assets.
• Conduct meaningful, targeted communication outreach including social and digital channels that enhance the reputation of our Company.
• Identify, develop and support unique storylines, media and thought-leadership opportunities to showcase our late-stage oncology pipeline assets.
• Prepare and brief oncology leaders on message delivery, media engagement and external speaking opportunities.
• Develop and communicate strategies, programs and materials for use by our company’s regions and subsidiaries worldwide.
• Serve as a liaison to third party groups (including advocacy organizations) and external experts (including researchers) and to trade and local news media.
• Manage high volume of materials (press releases, social media content, core response documents, etc.) through medical and legal review process.

Associate Director – Global Oncology Communications

Data Analyst

• Lead team to manage life cycle of digital data product, including use case identification, discovery all the way to development and maintenance.
• Translate use cases into implementation roadmaps to deliver high quality data products
• Establish common performance expectations and processes for data product owners, data analysts and scrum masters.
• Leverage data domain knowledge to shape the vision, strategy, and roadmap of domain level analytics ready datasets.
• Ensure implementation of Agile principles and best practices to continuously adapt to evolving business needs and user feedback
• Develop and maintain relationships with key vendor partners to shape the overall staffing strategy and continuously ensure high quality deliverables and optimized return on investment for the respective domain programs
• Demonstrate and role model key leadership behaviors, including: cross-functional and inclusive leadership, assertiveness and swift decision-making, active listening and strategic thinking
• Native AI/Gen AI mindset that continuously look at the way a data product is being built and optimize the process utilizing the full extent of the technology stack and advancements that are available and ensure the data products being built are Gen AI ready from the outset.

Associate Director, Data Analysis

Project Manager

• Participates as a key stakeholder on the Clinical Trial Teams (CTT) and collaborates closely with other functional area representatives to negotiate timelines and strategy for clinical supplies.
• Interacts with key partner organizations such as clinical development, regulatory, quality and other supply chain areas to address clinical supply and/or change management related topics.
• Responsible and accountable for establishing the timelines for clinical supply needs per study and providing the signal for sourcing, manufacturing, packaging, and distribution for our Company's development products and our Company's non-marketed products.
• Analyzes and anticipates clinical study risks as they relate to clinical supply chain deliverables and prepares, analyses, and/or develops mitigation strategies for review with clinical partners and senior leaders.
• Responsible and accountable for utilizing key tools/systems such as IRT & Microsoft PowerApps, SWMS, Veeva, MEDS, MyLearning, and other Microsoft Applications in the management of clinical supplies for assigned studies.
• Works directly in the SAP system to establish a consolidated, visible forecast for all study product needs (Bulk Drug Product and Clinical Finished Goods).
• Responsible for authoring clinical supply documentation in support of labeling and packaging activities as well as supply chain documentation to support critical CMC activities.
• Responsible for authoring the Clinical Supplies section of the study protocol as well as preparation and presentation of the clinical supplies information at Investigator Meetings for assigned protocols.
• Support the collection of clinical supply chain metrics and/or participate in critical non-pipeline activities.
• Participate in Interactive Voice Response (IVR) System development and User Acceptance Testing (UAT) for assigned studies.
• Participates in initiation and timely processing of change controls through collaboration with GCS Planning and other cross functional stakeholders and in accordance with established GCS planning SOPs/BPs and QMS Topic 3.4 Change Control Procedures and Work Instructions.
• Participates in authoring and timely processing of deviation records as well as supports deviation investigations as required.
• Participates in critical non-pipeline and compliance activities in support of GCS Planning (e.g., process improvement initiatives, subject matter expert roles, SOP/BP development/maintenance, cross functional projects, etc.)
• Participates in supporting regulatory agency inspections for assigned trials as required.
• Demonstrates high capability to solve unstructured problems, make informed risk decisions considering both technical & business risks, & influence portfolio decisions with facts and data.
• Demonstrates ability to balance strategy with ability for tactical execution and has strong ownership & accountability of assigned work.
• Focus on Customers & Patients. Make rapid, disciplined decisions. Demonstrates Ethics & Integrity.

Senior Specialist, Clinical Supply Project Manager – Protocol

• Drives execution of the annual V&I plan with medical affairs colleagues from key countries and regions including U.S.
• Acts as an empowered partner, making informed decisions with a strategic and agile mindset.
• Serves as the SME and connector across assigned therapeutic areas, translating global scientific platforms into actionable Medical Value Narratives (MVNs).
• Actively engages with country-level stakeholders—including medical advisors, payers, and scientific leaders—to ensure strategic alignment and support local data generation, congress planning, and advisory boards.
• Serves as the medical representative within Product Development sub-teams (including Clinical, V&I, Commercial, Publications, and Label), leveraging the V&I GMSA vision to drive strategic planning, outcome delivery, and tactical execution.
• Communicates pertinent information to stakeholders to inform and influence country and regional planning.
• Acts as the subject-matter expert, collaborating closely with V&I Outcomes Research, Policy, Commercial, and Market Access teams to identify and address opportunities and barriers in key countries.
• Serves as a strategic partner for Big Country Markets (U.S., China, Japan) with no RDMA role.
• Plays a pivotal role in bridging global strategy with local execution.
• Proactively collaborates with the US DMA and equivalent roles in China and Japan.
• Consolidates actionable medical insights from countries and regions.
• Engages with a network of international scientific leaders and other key stakeholders.
• Monitors external changing environment in partnership with the competitive intelligence (CI) team.
• Organizes global expert-input events (advisory boards and expert-input forums).
• Collaborates with Global Human Health (commercial) executive directors to inform of the GMSA portion of V&I plans to ensure alignment.
• Organizes global symposia and medical educational meetings.
• Supports key countries with the development of local data-generation study concepts and protocols when requested.
• Reviews Investigator-Initiated Study proposals from key countries (ex-U.S.) prior to headquarters submission.
• Manages programs (patient support, educational or risk management) to support appropriate and safe utilization of medicines.
• Demonstrates and champions our company’s Ways of Working, emphasizing innovation and focusing on the impact to the patient.
• Manages assigned budget with strong financial stewardship, ensuring delivery within a 3% variance.

Senior Director, Global Medical Affairs – Pulmonary Hypertension

Clinical Operations

• accountable for the execution of operational quality activities within the assigned therapeutic area
• oversee headquarters clinical quality operations and support clinical trial teams
• embed quality into the Company's sponsored trials
• ensure adequate vendor oversight and address quality issues
• develop quality plans to implement quality by design within clinical development programs
• maintain ongoing inspection readiness
• prepare for, manage and follow up on regulatory inspections

Clinical Quality Operations Manager, Oncology

• Participates as a key stakeholder on the Clinical Trial Teams (CTT) and collaborates closely with other functional area representatives to negotiate timelines and strategy for clinical supplies.
• Interacts with key partner organizations such as clinical development, regulatory, quality and other supply chain areas to address clinical supply and/or change management related topics.
• Responsible and accountable for establishing the timelines for clinical supply needs per study and providing the signal for sourcing, manufacturing, packaging, and distribution for our Company's development products and our Company's non-marketed products.
• Analyzes and anticipates project risks as they relate to clinical supply chain deliverables and prepares, analyses, and/or develops mitigation strategies for review with clinical partners and senior leaders.
• Participates in cross-functional initiatives/projects as either the project lead or stakeholder participant.
• Responsible and accountable for utilizing key tools/systems such as IRT & Microsoft PowerApps, SWMS, Veeva, MEDS, MyLearning, and other Microsoft Applications in the management of clinical supplies for assigned studies.
• Works directly in the SAP system to establish a consolidated, visible forecast for all study product needs (Bulk Drug Product and Clinical Finished Goods).
• Responsible for authoring clinical supply documentation in support of labeling and packaging activities as well as supply chain documentation to support critical CMC activities.
• Responsible for authoring the Clinical Supplies section of the study protocol as well as preparation and presentation of the clinical supplies information at Investigator Meetings for assigned protocols.
• Support the collection of clinical supply chain metrics and/or participate in critical non-pipeline activities.
• Participate in Interactive Voice Response (IVR) System development and User Acceptance Testing (UAT) for assigned studies.
• Participates in initiation and timely processing of change controls through collaboration with GCS Planning and other cross functional stakeholders and in accordance with established GCS planning SOPs/BPs and QMS Topic 3.4 Change Control Procedures and Work Instructions.
• Participates in authoring and timely processing of deviation records as well as supports deviation investigations as required.
• Participates in critical non-pipeline and compliance activities in support of GCS Planning (e.g., process improvement initiatives, subject matter expert roles, SOP/BP development/maintenance, cross functional projects, etc.)
• Participates in supporting regulatory agency inspections for assigned trials as required.
• Demonstrates high capability to solve unstructured problems, make informed risk decisions considering both technical & business risks, & influence portfolio decisions with facts and data.
• Demonstrates ability to balance strategy with ability for tactical execution and has strong ownership & accountability of assigned work.
• Focus on Customers & Patients. Make rapid, disciplined decisions. Demonstrates Ethics & Integrity.

Associate Director, Clinical Supply Project Manager – Protocol

Artificial Intelligence

• Find and Mitigate Risks in AI Projects as a Senior AI Analyst
• Leverage your skills and knowledge in AI systems to identify and assess potential risks and impacts, recommend appropriate mitigations, and prevent harm
• Work with business and technical stakeholders to understand business problems and AI risk
• Represent the global AI Ethics and Governance team - guide stakeholders on company governance processes and promote adoption of responsible AI
• Implement Explainable AI (XAI)
• Test and audit data sets, models and AI solutions for bias, fairness, and explainability using open-source and enterprise tools
• Support development and implementation of policy processes and further the field of AI ethics
• Research and stay on top of AI developments, best practices, and regulatory changes

Senior Artificial Intelligence Ethics and Governance Specialist

Software Engineer

• Leads and works independently as a team member on the development and scale up of processes or technologies of microbial, virus and cell cultivations, biomolecules concentration and purification and final formulation of veterinary vaccines and therapeutics.
• Leads and works independently as a team member on the transfer of processes or technologies of microbial, virus and cell cultivations, biomolecules concentration and purification and final formulation of veterinary vaccines and therapeutics to the production lines.
• Examines issues from diverse perspectives (safety, compliance, automation, equipment, process and people) in order to best understand and resolve the root cause.
• Collaborates and interfaces with R&D and Manufacturing and other departments to bring new products to market.
• Assures consistent application of standardized work, engineering and process tools

Senior Specialist, Engineering

Engineer

• Deploy, train and sustain core MPS/Lean Management System elements across FLEx and SLP
• Establish and maintain governance for CI execution, including metrics, CI portfolio management, gemba cadence, and follow-through
• Coach area operations leads, functional leaders, and first-line managers to own and operate the management system
• Lead and facilitate fact-based problem solving on complex operational and execution challenges.
• Embed MPS into existing governance and leadership routines across FLEx and SLP.

Continuous Improvement Engineer

Customer Success Manager

• Conduct Research & Analytical Deep-Dives
• Perform structured analysis of business processes, workflows, and pain points to identify and qualify AI opportunity areas across multiple business engagements.
• Gather, organize, and synthesize data from stakeholder interviews, operational metrics, industry benchmarks, and internal systems to build a fact base for each engagement.
• Conduct landscape scans of relevant AI technologies, vendor capabilities, and competitive applications to inform solution shaping.
• Translate Business Problems into AI-Ready Inputs
• Analyze and synthesize findings from stakeholder interviews, journey maps, and user research into clear problem statements, use cases, and desired outcomes.
• Document current-state workflows, user needs, pain points, and non-functional considerations required for Opportunity Assessment.
• Produce clear, well-structured analytical artifacts that translate business ambiguity into actionable inputs for AI and delivery teams.
• Perform Technically Grounded Opportunity Analysis
• Apply a strong understanding of AI, automation, data platforms, and cloud technologies to assess feasibility, complexity, and value potential of proposed AI solutions.
• Evaluate technical and data constraints by reviewing architecture documentation, data availability, and integration requirements alongside architects, data scientists, and engineers.
• Ensure proposed AI opportunities are grounded in technical reality and supported by evidence prior to handoff to delivery teams.
• Build Value Cases & Support PoC Planning
• Own the end-to-end value case for each assessed AI opportunity — from initial data discovery and analysis through building ROI models and business cases — providing the quantitative rigor needed to validate, prioritize, and advance initiatives into PoC.
• Define and document scope boundaries, assumptions, success metrics, and risk factors to support early PoC planning.
• Ensure analytical outputs are complete, coherent, and decision-ready, reducing friction during transition to delivery teams.
• Maintain traceability from business problem through value hypothesis to recommended path forward.
• Support Stakeholder Alignment & Reporting
• Build strong working relationships with business and IT stakeholders through clear communication, analytical credibility, and follow-through.
• Prepare executive-ready briefings, scorecards, and summary reports that distill complex analytical findings into clear recommendations.
• Contribute to positive stakeholder experiences by maintaining rigor, transparency, and momentum throughout engagements.

MSD