Research Scientist

• Lead a team in the development and execution of health economic and modeling strategies to support the value of the Company’s oncology portfolio
• Provide leadership, mentorship, and strategic direction to a team of 3–4 health economists
• Oversee the prioritization and development of high-quality global health economic models and tools to support market access, pricing, reimbursement, HTA submissions, and formulary decision-making across U.S. and international markets
• Collaborate with key countries and the regional team to adapt global models for local HTA, reimbursement, and formulary submissions
• Generate and communicate early health economic insights to inform development and commercialization strategies
• Build strong partnerships with internal stakeholders to ensure modeling strategies align and support the overall product development and value evidence strategy and implementation
• Develop and maintain relationships with external thought leaders in health economics, decision sciences, and health policy to enhance scientific credibility, inform strategy, and position our company as a leader in the field

Senior Principal Scientist, Outcomes Research

Scrum Master

• Facilitate Agile Events: Organize and facilitate all agile events ensuring that the events are positive, productive, kept within the timebox and ensure teams follow the agile spirit and practice.
• Coaching and Mentoring: Mentor the team members and explain to them using the agile methods, fostering a culture of continuous improvement.
• Team Development: Help teams identify and remove impediments, promoting self-organization and accountability.
• Stakeholder Collaboration: Work closely with Product Owners & Managers and other stakeholders to ensure alignment on goals and priorities.
• Metrics and Reporting: Track and report on team performance metrics, using data to drive improvements and inform stakeholders.
• Conflict Resolution: Mediate conflicts within teams and between teams and stakeholders, ensuring a collaborative environment.
• Risk Management: Identify potential risks and issues, facilitating discussions to develop mitigation strategies.

Senior Technical Project Manager – Scrum Master

Operations

• Lead the Technical Operations team in support of the manufacturing of Active Pharmaceutical Ingredients, intermediates, and drug product intermediates at external contract manufacturing facilities in the region
• Provide leadership and expertise in technical oversight, portfolio management, continuous improvement, talent development and upskilling organization capabilities
• Ensure technical excellence in routine supply support to contract manufacturers
• Lead the technical efforts required for enhancing competitiveness through targeted process optimization
• Drive organizational capability in Proactive Process Monitoring to enable robust manufacturing operations & early detection of process issues
• Foster a community of sharing, curiosity, learning, and end-to-end mindsets for new technologies, ways of working & new product introductions
• Create a robust technical network of internal and external resources, rapidly deployable to solve complex problems in a cross-functional manner

Director, Chemical Technical Operations

Procurement

• Lead the sourcing of nonclinical safety studies (GLP and non-GLP) for inclusion in regulatory submissions that support clinical development and/or marketing authorization.
• Interact directly with external client service representatives, management and other key personnel (e.g., Study Directors) at multiple CROs for study coordination, planning of initial protocol development, coordinating study report review, and defining project study timelines.
• Partner with Study Monitors and internal functional group experts to facilitate the planning, development, tracking, and reporting timelines of nonclinical outsourced studies.
• Participate in selection of CROs, including qualification/scientific assessments and the tracking of vendor performance.
• Monitor CRO performance and drive consistency in processes, quality, and communication.
• Partner with internal stakeholders, our Research & Manufacturing division, Finance, and NDS leadership to develop, track, and forecast our sourcing budget, ensuring alignment with NDS priorities, accurate financial planning, and proactive identification of risks and variances.
• Oversee operational readiness for study initiation, including contracts, materials, and documentation.
• Maintain timely, accurate tracking of studies and provide clear status updates to internal stakeholders on externally outsourced work.
• Identify and implement process improvements to enhance sourcing efficiency and quality.

Associate Director, Non-Clinical Outsourcing

Project Manager

• Analyze, design, and maintain compliant and efficient clinical supply chain networks for assigned clinical studies
• Ability to collaborate cross-functionally with Clinical Supply Planning, Clinical Operation, Country Operations, CMOs, Regulatory, Trade Compliance, and third-party providers
• Ensure readiness of internal and external depots/warehouses for global distribution, including verification of trade and regulatory data, temperature control requirements, shipping materials and compliance with GMP and GDP standards
• Partner with internal and external stakeholders to resolve clinical supply-related issues in a timely and effective manner

Senior Specialist, Project Management – Logistics

Director

• Drive a platform-centric security strategy, ensuring that enterprise applications and AI-enabled systems are built and operated securely at scale.
• Serve as a hands-on leader, translating strategy into production-grade capabilities that reduce risk, enable innovation, and protect enterprise data and intellectual property.
• Lead and develop a high-performing team responsible for security across strategic platforms, including AI systems, SaaS applications, and PaaS/cloud-native environments.
• Define and execute the security strategy for enterprise platforms, aligning with business priorities and risk reduction objectives.
• Establish and scale SaaS security capabilities, such as SaaS Security Posture Management (SSPM), data governance, and third-party platform risk controls.
• Drive automation and engineering-first approaches to reduce manual controls and improve scalability of protection across thousands of applications and services.
• Partner with Legal, Privacy, Risk, and Compliance teams to ensure alignment with regulatory and data governance requirements.

Associate Director – Strategic Platforms

Compliance

• responsible for the review and approval of all US promotional materials
• serving as the promotional regulatory expert with legal, medical and commercial colleagues
• serve as the liaison and manage correspondence with FDA’s promotional review divisions OPDP/APLB
• propose creative, effective, and compliant regulatory strategies and solutions to challenging promotional concepts
• provide regulatory consultation in the development and implementation of US marketing strategy and promotional programs
• support the US commercial teams by participating in strategy discussions and providing regulatory guidance
• provide promotional regulatory input on concepts and draft materials
• actively participate in labeling and global regulatory team meetings
• maintain current awareness and understanding of FDA advisory correspondence and regulations
• ability to take on more complex projects and provide promotional regulatory training and coaching to team members

Assoc Director, Regulatory Affairs – Advertising and Promotion

Financial Planning and Analysis

• Provide financial planning, forecasting and analytical support to our Research and Development Division Global Clinical Supplies
• Modeling and forecasting spend related to freight, warehousing and distribution, external packaging and labeling, shipping supplies, contractor and headcount resources
• Provide forecasting and analytical support for GCS capital expenditures
• Ad hoc data analysis and projects in support of Global Clinical Supplies
• Develop and participate in team presentations associated with any financial and/or operational review with client areas being supported
• Support project team decision making by providing relevant financial information and insight
• Play a central role in developing the Budget, Long Range Operating Plan, Quarterly Forecasts, and monthly/quarterly close activities
• Gain end-to-end exposure to the drug development process and the Research & Development pipeline while gaining relevant experience supporting functions in Global Clinical Supplies
• Think strategically and identify opportunities to influence various parts of the GCS organization to drive efficiencies in the planning and forecasting process
• Further develop creative thinking and problem-solving skills
• Gain experience in change management and project management
• Increase personal network through engagement with other key business partners (Global Clinical Development Finance, Global Clinical Supplies, Project Management, Supply Chain Management, Procurement, etc.)

Senior Financial Analyst

• Develops professional relationships and engages with national and regional SLs to ensure access to medical and scientific information on areas of therapeutic interest and Company products
• Conducts peer-to-peer scientific discussions and maintains a reliable presence with those SLs to ensure they have a medical contact within the company
• Addresses scientific questions and directs SL inquiries on issues outside of Regional Medical Scientific Director scope (e.g., grants) to appropriate company resources consistent with applicable policies
• Maintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI)
• Upon request from Global Center for Scientific Affairs (GCSA), initiates discussions with SLs and/or potential investigators that include scientific/data exchange within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trial
• Enhances the comprehension of the scientific foundations and goals of investigator-sponsored research
• Identifies barriers to patient enrollment and retention efforts to achieve study milestones
• Recommends study sites and identifies potential investigators to participate in phase II-III clinical development programs, conducts Site Initiation Visits (SIVs), and detects barriers to patient enrollment and retention efforts to achieve study milestones
• Addresses questions from investigators and provides information regarding participation in company-sponsored clinical studies
• Engages in scientific congresses and medical meetings, facilitates scientific and data exchange for both internal and competitor data
• Gathers feedback, data, or information during routine activities that can help the company better comprehend medical or scientific needs, priorities, or concerns of SLs and/or patients

Oncology Regional Medical Scientific Director – Breast

• Leads the delivery of analysis and reporting tools, processes, platforms, and training for Biostatistics and Research Decision Sciences (BARDS) staff supporting all clinical trial phases and therapeutic areas.
• Partners with Statistics and Statistical Programming leaders, aligns work to the company scorecard, and collaborates with stakeholders and functional service partners.
• Manages managers and builds high-performing teams by recruiting, hiring, developing, and evaluating staff.
• Contributes to the broader vision and strategy of the Statistical Programming organization.
• Maintains current knowledge of regulatory guidance and submission standards.
• Manages team headcount and budget, and collaborates with vendors.

Executive Director, Statistical Programming

Medical Director

• Develops ongoing professional relationships with key decision makers in organized health systems to ensure access to medical and scientific information on the full oncology product portfolio and areas of therapeutic interest
• Develops strategic account plans in partnership with the Integrated Account Management (IAM) Account Executive teams and executes medical activities in alignment with agreed plan
• Serves as the primary resource for market dynamics within the territory to understand decision makers’ evolving information needs to feed into the ongoing value-proposition development process for oncology product and non-product offerings
• Effectively communicates and coordinates with Regional Medical Scientific Director regarding medical and scientific support needs in key health systems accounts
• Serves as a resource for the HSO MAD Team Lead, HSO Executive Director Medical Affairs, and other members of Country Medical Affairs on other relevant strategic planning
• Attends and supports scientific and medical meetings and prepares post-meeting deliverables

Health Systems Oncology Medical Affairs Director

• Leads, manages and provides scientific and strategic direction to teams leading the development and execution of high-quality evidence strategies and plans
• Ensures that the annual Value & Implementation (V&I) plans for the therapeutic area (TA) deliver research data and evidence for use in markets with impending launches
• Helps achieve / sustain reimbursement and market access for the TA
• Accountable for the development and delivery of innovative, timely, robust health outcomes and economic evidence to support and optimize market access, pricing, reimbursement, HTA, formulary listing and promotion of our company's products
• Develops a strong matrix relationship with clinical development, medical affairs, market access, commercial, and key markets to ensure that clinical, commercial and access strategies fully reflect payer/ HTA requirements

Executive Director, Outcomes Research – Pediatric Vaccines

Software Engineer

• Oversee and coordinate clinical database activities across multiple clinical programs, including review of eCRFs, edit check specifications, and database development
• Ensure adherence to clinical database standards, SOPs, and process guidelines
• Plan and manage timelines for database deliverables; identify and escalate risks appropriately
• Interface with study teams and stakeholders to integrate requirements into deliverables
• Align with CDS leadership to ensure consistency of technical strategies and execution
• Lead and participate in improvement initiatives, including task forces, automations, and exploration of emerging digital capabilities (e.g., advanced analytics, AI-enabled tools)
• Contribute strategies and innovative solutions to enhance processes and increase productivity, including the appropriate use of automation and data-driven approaches
• Support testing and evaluation of new systems, tools, and capabilities
• Coordinate and contribute to CDS technical initiatives that improve efficiency and scalability
• Serve as subject matter expert (SME) in clinical database and EDC activities, including database development and data integration
• Increase functional effectiveness by supporting efforts to simplify and standardize processes, including identifying opportunities for automation and improved data workflows
• Provide technical guidance, best practices, and knowledge sharing across the team and broader organization
• Provide oversight and guidance to Clinical Database Developers
• Support recruitment, onboarding, mentoring, and technical development of team members
• Contribute to performance management input and capability development planning
• Lead or contribute to functional and cross-functional meetings
• Communicate clinical database processes, requirements, and risks effectively to stakeholders and vendors
• Support alignment, decision-making, and continuous improvement efforts

Associate Director – Programmer, AI & Automation

• Drives execution of the annual V&I plan with medical affairs colleagues from key countries and regions with a focus on the US.
• Acts as an empowered partner, making informed decisions with a strategic and agile mindset.
• Serves as the subject matter expert (SME) and connector across assigned therapeutic areas.
• Actively engages with country-level stakeholders—including medical advisors, payers, and scientific leaders.
• Serves as the medical representative within Product Development sub-teams.
• Communicates pertinent information to stakeholders to inform and influence country and regional planning.
• Collaborates closely with V&I Outcomes Research, Policy, Commercial, and Market Access teams.

Senior Global Director Medical Affairs – Genitourinary Malignancies

Translator

• serve as expert PK/PD modeler in cross-functional teams, to make model-informed decisions about drug discovery, modality selection, and dose prediction across therapeutic areas
• integrate in vitro and in vivo data to build PBPK, quantitative systems pharmacology (QSP), or other mechanistic modeling platforms of drug disposition and pharmacology, to support forward / reverse translation for both established and novel therapeutic targets
• guide software developers in the design of automated workflows for implementing modeling platforms, to inform human PK/PD and dose projections
• collaborate across the PDMB organization to develop modeling and simulation strategies to identify and optimize drug candidates
• provide scientific guidance and cross-functional supervision to a team of growing scientists
• mentor / supervise junior colleagues to perform the above duties and to grow the above capabilities.

MSD