Marketing

• Define and execute the global commercial disease and asset strategies for the Bladder Cancer portfolio.
• Setting and leading global Bladder Cancer portfolio strategy.
• Ensure strategies are informed by robust insights into customers, competitors, and the evolving standards of care across all stages of disease in Bladder Cancer.
• Drive global launch and lifecycle management for assets in Bladder Cancer.
• Provide commercial leadership and input into clinical development programs, target product profiles, and evidence generation plans for assets in Bladder Cancer.

Executive Director, Global Oncology – Bladder Cancer

Procurement

• Responsible and accountable for sustaining existing and developing new cooperation frameworks across three stakeholder groups.
• With Procurement Colleagues: Participates/leads teams of global, regional & local representatives to develop and implement strategic source plans as well as to ensure alignment on key initiatives and priorities for broader Marketing services categories.
• With Business Partners: Identifies and engages with critical stakeholders and partners to define and meet or exceed business requirements and identify and manage profit plan savings targets.
• With Suppliers: Responsible for building relationships with Global, International and Enterprise suppliers and managing key supplier performance against business requirements using proven processes.
• Design, planning and implementation of actions and projects in connection with Sourcing Management Process or strategic goals pursuant to develop, improve, sustain or reposition our Company's relationship with critical/strategic suppliers.

Director, Global Procurement – Marketing Operations

Research Scientist

• Lead Human Factors Project Work (Execution and Strategy), including, but not limited to: Establish and own HF strategy from early concept through validation and post-market for devices and combination products
• Build HF plans and study roadmaps; select methods (user research, task/use-error analysis, risk mitigation, formative/summative usability testing)
• Turn user insights into design inputs for device UI, packaging, labeling, and IFU; guide intuitive, safe designs
• Partner with marketing, program management, clinical, safety, regulatory, manufacturing, packaging, and labeling to integrate HF and manage risk
• Lead regulatory deliverables: HF protocols/reports, linkage to risk management (ISO 14971), hazard/use-related risk analyses, and submission materials (FDA, EU MDR)
• Maintain and manage compliant HF documentation and traceability; ensure audit readiness
• Monitor post-market use-related issues and drive corrective actions and training
• Define and continuously improve HF process, standards, and templates per IEC 62366-1 and FDA guidance
• Create reusable platform methods for needs discovery, user profiling, task analysis, and use-related risk assessment
• Provide portfolio-level guidance for UI, labeling, and IFU to reduce use-related risk
• Train cross-functional teams on HF practices and compliant documentation
• Establish metrics and feedback loops (study quality, defects, post-market signals) to prioritize improvements
• Maintain centralized HF libraries and tools to enable reuse and speed development
• Stay up-to-date with the latest advancements in human factors within the regulatory and industry landscape, and have the ability to represent our company in external communities and exert influence

Associate Principal Scientist, Human Factors

• Provide strategic and scientific leadership in the design, execution, analysis, and communication of clinical biomarker strategies across immune-mediated therapeutic portfolio
• Drive decision-centric biomarker strategies that connect drug mechanism, disease biology, precision medicine
• Lead and shape integrated biomarker strategies across discovery, early- and late-stage clinical programs
• Serve as the biomarker strategy lead within cross-functional program teams
• Inform portfolio strategy by advancing biomarker-driven insights
• Translate disease biology into clinically actionable biomarker strategies
• Drive selection and application of innovative biomarker approaches
• Collaborate effectively across disciplines to integrate scientific perspectives into cohesive strategies
• Champion biomarker analysis plans and provide critical scientific input to interpretation of complex datasets

Senior Principal Scientist, Translational Clinical Biomarkers

Project Manager

• Partner with lead Project Managers to accurately reflect team strategy and plans in enterprise project management systems.
• Build, maintain, and analyze integrated development project schedules (timelines and deliverables) in alignment with established standards and in collaboration with lead PMs and the PMO.
• Support multiple projects across all stages of development (preclinical through lifecycle management), therapeutic areas, and modalities; projects may vary in priority, pace, complexity, and include alliance partners.
• Understand schedule deliverables, dependencies, and interdependencies; proactively identify, communicate, and help resolve risks, conflicts, and constraints.
• Ensure high data quality and adherence to established scheduling, planning standards, specifications, and systems.
• Create new project schedules for programs entering the pipeline, as needed.
• Serve as first-line technical support for project planning systems, including troubleshooting and system build guidance.
• Share scheduling expertise by mentoring new colleagues and promoting best practices.
• Contribute to continuous improvement by participating in pilots for new tools, processes, and planning approaches.
• Build strong working relationships and collaborate effectively with stakeholders within and outside the department.
• Participate in relevant training to develop knowledge of drug development, project management capability, and leadership skills.

Associate Specialist, Project Management – Research & Development, Scheduling

• Lead in value evidence teams in Women’s Cancer and contribute to value evidence strategies.
• Obtain senior management approval of evidence generation plans.
• Provide outcomes research leadership on cross-functional regional and global teams.
• Critically assess drivers and barriers to reimbursement and market access, and provide input into clinical, regulatory, payer/access, marketing and evidence generation strategies and programs.
• In collaboration with internal teams and external partners, design studies, author study protocols, develop measurement questionnaires, case report forms, data analysis plans, final study reports, scientific presentations, and publications.
• Responsible for study-related contracting, and budgets.
• Develop supplementary clinical data package in close partnership with markets and HTA statistics group for submission to HTA agencies.
• Support country affiliates to understand local evidence generation needs, adapt health economic evaluations, customize outcomes research documents, such as protocols and reimbursement dossiers, according to local requirements.
• Work closely with cross functional teams to effectively communicate outcomes research and health economic modelling data internally and to external stakeholders.
• Maintain awareness of new scientific and methodological developments within therapeutic area.
• Build relationships with scientific experts worldwide.
• Present outcomes research data at national and international congresses and publish articles in scientific journals.

Principal Scientist – Outcomes Research

Clinical Operations

• Drive scientific planning, strategy, and execution of Phase 1-4 clinical studies
• Collaborate with global cross ­functional team members including clinical directors and study managers
• Responsible for the clinical/scientific execution of clinical protocol(s)
• Serves as the lead clinical scientist on the clinical trial team
• Collaborates with the Medical Writer on clinical/scientific and regulatory documents
• Partners with Study Manager on study deliverables
• Participates in the set up and design during study start up
• Lead medical monitoring team in review and interpretation of clinical data/medical protocol deviations

Associate Principal Scientist, Clinical Operations

• Own the end-to-end integrated brand/franchise strategy across priority audiences and channels; translate insights into clear strategic choices, annual priorities, and measurable outcomes.
• Develop the Global HCC/HCP strategy, incorporating our Company's marketing framework to include segmentation, value proposition, messaging, and go-to-market strategy for HCCs and HCPs.
• Ensuring all tactics align to the customer experience plan and achieve desired customer experience.
• Lead global campaign evolution and delivery, in partnership with key markets and regions.
• Partner closely with other members of the PrEP team to ensure consistent integration and seamless brand experience between and across customers, markets and touchpoints.
• Set omnichannel strategy and channel roles (paid/owned/earned), inclusive of social and digital tactics; partner with analytics to optimize journeys, content, and media based on performance learning.
• Steward brand identity and trademark strategy by ensuring consistent naming, messaging, and visual standards across materials; coordinate required reviews and maintain version control and governance.
• Lead the marketing contribution to the annual profit plan by aligning strategic initiatives and investments to Franchise priorities; articulate risks/opportunities, investment choices, and scenario options for leadership reviews.
• Integrate SDOH considerations into strategy development and execution to reduce barriers to care; coordinate cross-functional initiatives and external partnerships that support access and outcomes.
• Identify capability gaps and lead learning plans for launch readiness, cross-functional teams and field stakeholders (e.g., disease state, product, customer insights, digital fluency); ensure tools and playbooks enable consistent execution.
• Lead data and analytics strategy and execution to address key business questions and strategic decision making.
• Partner with market access and trade to shape pharmacy channel strategy (e.g., distribution, patient support, pull-through); identify access friction points and develop tactical plans to improve initiation and persistence.

HCC/HCP Strategy Lead, Global Marketing – HIV Pre-exposure Prophylaxis

Compliance

• Partner with business to ensure compliance with laws and ethical standards
• Provide compliance counsel for HH Business Units
• Execute AI risk assessments and establish risk mitigation controls
• Develop policies and guidance documents
• Collaborate with Global Privacy Office
• Provide end-to-end compliance support to Marketing and Sales personnel
• Member of Franchise Marketing and Sales teams
• Oversee management certifications and communication tracking
• Support audit processes and revise compliance policies

Commercial Compliance Officer

Risk

• 開発品安全性業務
• 申請時電子添文「使用上の注意」、J-RMP(安全性検討事項、安全性監視計画、リスク最小化策)の立案、作成
• CTDの関連パート作成、審査対応
• 製造販売後調査プロトコル作成
• 最適使用推進ガイドライン(GL) 作成・改訂
• 市販品安全性業務
• 集積情報等にもとづく安全確保措置の検討
• 電子添文、J-RMP改訂要否検討及び改訂案作成(PMDA、米国本社及び国内他社等との交渉/相談含む)
• 情報提供資材の作成・改訂
• 製造販売後調査のプロトコル改訂
• 最適使用推進GL改訂
• 安全性定期報告書及び再審査申請資料の安全性パート作成
• 市販後安全対策全般に関する外部医学専門家とのコミュニケーション、各学会対応

Sr. Specialist, R&D PV Safety Risk Management

People Operations

• 開発品安全性業務
• 申請時電子添文「使用上の注意」、J-RMP(安全性検討事項、安全性監視計画、リスク最小化策)の立案、作成
• CTDの関連パート作成、審査対応
• 製造販売後調査プロトコル作成
• 最適使用推進ガイドライン(GL) 作成・改訂
• 市販品安全性業務
• 集積情報等にもとづく安全確保措置の検討
• 電子添文、J-RMP改訂要否検討及び改訂案作成(PMDA、米国本社及び国内他社等との交渉/相談含む)
• 情報提供資材の作成・改訂
• 製造販売後調査のプロトコル改訂
• 安全性定期報告書及び再審査申請資料の安全性パート作成
• 市販後安全対策全般に関する外部医学専門家とのコミュニケーション、各学会対応

Associate Director, R&D PV Safety Risk Management

Clinical Research

• Ensures the implementation of clinical trials in compliance with standards
• Acts as primary site contact and manager throughout clinical research phases
• Develops strong site relationships
• Performs site management and monitoring activities
• Participates in site selection and qualification activities
• Conducts site visits and prepares reports in a timely manner
• Communicates with investigators and site staff
• Manages documentation in CTMS, eTMF, and other systems

Associate Specialist, Clinical Research

• Leads a procurement team responsible for providing sourcing & supplier management support
• Develops procurement strategy and guides global category management
• Maintains strong relationships with key business leaders across R&D

Executive Director, Procurement

Director

• The Market Research Associate Director (Hybrid) will be a main point of contact for their assigned areas of responsibility for our product's marketing / commercial team
• Plan, prioritize, manage, and execute a scope of work within the Oncology Business Unit
• Support the Pan-Tumor franchise and other tumor areas as needed
• Provide strategic input to the extended global team via primary market research projects and secondary data analysis
• Proactively define business questions and opportunities
• Identify strategic insights, and recommend actionable business solutions
• Demonstrate consistently strong leadership skills
• Work independently in a rapidly changing environment with a transformational mindset, cultural awareness and resiliency to change
• Develop and oversee execution of an assigned portion of the global market research plan within the product franchise

Associate Director, Market Research

• Lead external quality management and oversight of third-party manufacturing partners and CMOs
• Serve as the Quality point of contact for external partners and internal stakeholders
• Lead external manufacturing Quality team in Mexico and Canada for review, packaging and release for all local and imported products
• Ensure partner compliance with GMP requirements, Quality Agreements, and commercial commitments
• Oversee batch review, product release, change control, validation, audits, and remediation activities
• Support quality system improvement, risk management, and continuous improvement initiatives
• Manage team performance, budget, and headcount planning
• Partner cross-functionally to support operational excellence, compliance, and supply continuity

MSD