Operations

• Provide functional area operations leadership and direction across the assigned organization; define policies, governance frameworks, and forecasting methodologies; provide operations oversight to monitor consistent execution, quality, and compliance with functional area business processes.
• Represent the functional area portfolio, resource and operations management in enterprise forums; communicate options/risks/trade-offs; serve as escalation point for issues arising within assigned teams or geographies.
• Lead or sponsor global initiatives to improve operational efficiency, continuous improvement leveraging automation / AI, quality by design, and change management in alignment with Global Data Management & Standards (GDMS) priorities.
• Approve headcount/JD plans and funding cases, and oversee real-time, compliance-driven workload balancing / allocation across geographies - including proactive capacity planning, absence/holiday coverage, and surge redistribution - to ensure business continuity and on-time delivery to regulatory and business timelines.

Senior Director, Clinical Data Management, Portfolio, Operations

Marketing

• Own and refine the HCP Endometrial strategy across customer segments to maximize commercial performance and align field and non-field tactics to drive business priorities.
• Lead and manage the evolution of L3 for endometrial portfolio (KN868 and launch of C93) including identification of new strategic choices, segmentation, messaging evolution, and resource needs/development.
• Lead market research and activity metric/performance monitoring to inform strategic and execution opportunities.
• Collaborate with field leaders, field execution team, ORTs, and Team 2 marketing to support pull through of executional excellence.
• Translate customer segmentation insights into targeted personal and non-personal promotional plans that positively impact the business.
• Establish and report on clear KPIs to measure promotional effectiveness, market share movement, and commercial ROI; iterate plans based on results and changing market dynamics.
• Manage and hold team accountable for timely delivery, creative excellence, budget discipline, and measurable impact.
• Partners with Global Marketing, Precision Medicine, DHH, Finance, Forecasting and other stakeholders to monitor the evolving treatment landscape, inform scenario planning, and support counter-competitive strategy development when appropriate.
• Manage the Endometrial Cancer budget

Associate Director, US Oncology Marketing HCP Strategy – Endometrial Cancer

Business Analyst

• Support digital products and platforms that enable our Company's Research & Development laboratory workflows
• Partner with R&D scientists and technical teams to analyze laboratory workflows
• Act as a subject matter expert (SME) for laboratory systems
• Support the implementation and lifecycle management of laboratory systems

IT Product/Business Analyst

Vice President

• planning and directing clinical research activities involving new or marketed drugs for oncology indications
• manage and oversee the entire cycle of clinical development, including study design, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation
• evaluating pre-clinical and translational work for the purpose of generating early clinical development plan and Investigational New Drug applications
• developing clinical development strategies for investigational or marketed vaccines
• monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed vaccines
• analyzing and summarizing the clinical findings from studies
• participation in internal and joint internal/external research project teams relevant to the development of new compounds,
• mentoring and career development for direct reports

Associate Vice President, Global Clinical Development, Oncology Assets

Content Marketing Manager

• Actively engaging with key stakeholders in creating and adapting the V&I Planning and Scientific Platform
• Developing and adapting annual GSVC plans for one or more products and disease states aligned with the annual V&I Plans
• Leading the development, review, approval, and communication of individual GSVC content within V&I
• Authors the development of GSVC content that aligns to annual GSVC plan(s) and V&I Plans and Scientific Platform
• Reviews GSVC materials to ensure they are relevant, scientifically accurate, and consistent with cited appropriate scientific literature
• Ensures appropriate stakeholders are engaged in the development, review and approval of GSVC materials
• Communicates to key stakeholders about GSVC-approved content
• Leads product-related projects/initiatives that directly impact the franchise/product strategy and objectives to meet external customer needs
• Helps GSVC P3 job role staff develop within their functional roles

Associate Director, Global Scientific & Value Content – Payor

Data Analyst

• Partners with internal stakeholders to understand the needs of V&I.
• Identifies appropriate data sources to address the needs of V&I.
• Ensures high quality, rigorous and readily interpretable deliverables.
• Develops data visualizations and presentation decks to communicate findings.
• Provides recommended actions with stakeholders from senior and executive leadership teams.
• Contributes toward a collaborative environment where the Medical Data Analytics Center team maintains an entrepreneurial spirit.
• Keeps abreast of the latest trends in the field through continuous learning and proactively championing new methods to solve critical and emerging V&I problems.
• Collaborates and partners with peers in other functions on cross-functional analytics projects and to drive efficiencies in developing innovative quantitative analyses.
• Manages external vendors.
• Develops and owns scalable-analytic products that fulfill stakeholders needs.
• Designs and develops analyses to draw inferences and conclusions to inform decision-making for V&I.

Associate Director, Data Enablement – Medical Data Analytics Center

Director

• Leads a large investigator-initiated studies program in partnership with late-stage development teams in Medical Affairs while also supporting early-stage development teams
• Drive a credible and informed scientific dialogue with global Scientific Leaders in Pulmonary Hypertension related areas
• Partner with colleagues in Research & Development GCD to execute the Scientific Leadership strategy in alignment with the end-to-end pulmonary hypertension scientific strategy
• Partners with Medical Affairs leadership to develop the global Value Evidence and Medical Planning strategy across designated therapeutic areas
• The EDSA has a key role at major congresses, including, but not limited to, facilitating daily debriefs, engaging with Scientific Leaders (SLs), and producing comprehensive congress summary reports
• Responsibility for both internal and external commitments, with an emphasis on external scientific engagements

Executive Director, Scientific Affairs – Pulmonary Hypertension

Infrastructure Engineer

• Design, develop, and maintain advanced backup and recovery solutions using tools such as Cohesity, AWS Backup, Azure backups, Commvault
• Develop and implement automated solutions for backup and recovery processes to enhance efficiency and reduce manual intervention (preferably python, Ansible, PS, GitHub Actions)
• Create and manage self-service features for customers to facilitate their own backup and recovery tasks, improving user experience and operational efficiency (API based using python, Ansible, PS, GitHub Actions)

Infrastructure Engineer – Hybrid Data Protection

• Provides clear direction, vision and alignment to USMA strategy and enterprise priorities.
• Fosters team cohesion, morale and resilience through effective communication, recognition and accountability.
• Creates a culture of trust and psychological safety (i.e., safe to speak up) that promotes continuous learning and growth.
• Empowers team members to lead, take ownership, and drive innovation across the organization.
• Serves as a trusted partner to senior leaders, offering insights that shape decisions and strategic planning.
• Sets clear, measurable objectives aligned to USMA goals and monitors progress against established performance expectations.
• Ensures accountability by the disciplined use of performance documentation, highlighting impact, and addressing gaps in a timely manner.
• Models integrity and ensure team adherence to compliance, medical governance, and regulatory requirements, fostering a culture of transparency and accountability.
• Contributes to annual budget planning and manages team budget, acting as a financial steward of company resources.

Senior Director, Team Lead, US Medical Affairs, COPD

Research Scientist

• Provide regulatory leadership, oversight, and strategy to a team of Regulatory CMC Professionals in developing global Regulatory CMC strategy and executing submissions related to small molecule, development products.
• This includes preparation of applicable IND/CTA’s, Agency Background Packages, Worldwide Marketing Applications (including Most of World applications), and transfer strategy to post-approval grp. for further submissions occurring within several years post-launch in the major markets.
• This role may also directly support a project in a similar capacity; however, the primary focus of the position is providing direction to the team members that are responsible for developing and overseeing implementation of regulatory strategies, and making decisions that ensure high quality, accuracy, and high likelihood of approval of all regulatory submissions.
• This includes assessing CMC changes during development, defining regulatory requirements, developing CMC regulatory strategies demonstrating sound regulatory insight, ensuring a balanced approach to regulatory risk, understanding the impact to the business, utilizing regulatory intelligence, and incorporating knowledge of the changing regulatory environment.
• Be responsible for proactive and timely communication of regulatory risks, challenges, and opportunities to management to help address them in a systematic and thoughtful manner.
• Develop, execute & provide oversight of regulatory initiatives & strategies of significant complexity and apply exceptional ingenuity to solve problems and mitigate potential regulatory challenges.
• Drive the application of regulatory strategies and concepts across multiple disciplines and multiple organizations, including working directly with Senior Leadership in these areas.
• Embody our Company's Values and Leadership Behaviors in day-to-day activities and serve as an example by practicing them consistently.
• Continuously evaluate and develop talent within the team and prepare a succession plan.
• Use recognition and rewards to promote team and organizational collaboration.
• Set a vision for the team and hold employees accountable for the execution of departmental policies and procedures.
• Manage resources and prioritization within assigned areas.
• Actively sponsor employees who lead and participate in our Company's initiatives.
• Develop strong collaborative relationships with stakeholders and partners across the organization.
• Represent the department’s needs and positions in senior leadership forums.
• Develop and maintain expert knowledge of current global regulatory CMC requirements for IND/CTA submissions, and original registrations.
• Identify and resolve technical and operational problems associated with regulatory strategy and submissions using rapid, disciplined decision making; collaborate with peers to resolve cross-functional obstacles using excellent critical thinking skills.

Principal Scientist – Regulatory Affairs, CMC

Full-stack Engineer

• Collaborate with Product Managers and designers to translate product goals into technical solutions, with a keen focus on value, business outcomes, and user experience.
• Define and lead product architecture, ensuring scalability, performance, and maintainability.
• Lead the product technical design and implementation of product features, ensuring alignment with product vision and customer needs, along the full product lifecycle.
• Drive architectural decisions for the product, in partnership with functional technology leaders, and advocate for best practices in hardware development, software development, data, AI, testing, and deployment.
• Partner with functional R&D leads to support and grow engineers, fostering a culture of continuous learning, innovation, and technical excellence.
• Mentor and coach engineers, modelling best practices across hardware, software, and data engineering.
• Collaborate cross-functionally with R&D, Product Management, Design, Supply Chain and Manufacturing, Marketing, Sales, and Customer Success to ensure alignment and delivery.
• Facilitate effective communication and collaboration across cross-functional teams, connecting technical teams directly with customers as appropriate.
• Ensure speed to market of our products, while maintaining appropriate focus on quality, scalability, and performance.
• Identify technical risks early and proactively define mitigation strategies.

Director R&D Technical Lead – Animal Health

• Work with APLs to develop and implement the commercialization analytical strategy across testing nodes.
• Participate in significant investigations across the viral vaccines franchise.
• Provide Subject Method Expertise to QC analysts and supervisors, assess impact of proposed changes and deviations.
• In partnership with the AWG and network QC labs, support definition of the opportunities for improvement/investment in equipment and technology required to drive assay modernization and implement harmonized network solutions.
• This includes working with our Digital manufacturing Division and LMAS team for assay digitization with harmonized data capture.
• In partnership with the BCR hub, develop short and mid-term strategy for sustainability in BCR inventory and antisera generation needed to support all testing laboratories in the network and connect BCR performance with assay performance as noted above.
• Provide SME support to APLC gap assessments of key methods to drive improved and sustainable robustness.
• Ensure method performance data are presented, discussed and actions developed at analytical working group meetings as appropriate.
• Collaborate across the internal network, external partners, international governments and/or contract manufacturing and research organizations (CMO/CRO) to ensure uninterrupted supply
• Escalate key assay challenges to management in a timely and concise manner.
• Support RTQs, PAI readiness and audit observations

Associate Principal Scientist, Analytical R&D

• Under the guidance of a senior leader, manage real world and economic evidence activities
• Execute prospective and retrospective observational studies
• Develop American Managed Care Pharmacy (AMCP) dossiers for US payers
• Collaborate with internal teams and external partners to design studies and author protocols
• Supervise external vendors or partners

Associate Director, Outcomes Research

Engineer

• Collaborate with formulation scientists, engineers, operations staff, quality representatives, and other team members
• Provide technical input on sterile processes from a facility and operational standpoint
• Ensure timely availability of clinical supplies and development batches
• Monitor the achievement of batch planning and execution progress
• Perform key batch activities, such as authoring the batch record and coordinating transfer of batch inputs
• Prepare and facilitate key team meetings

Process Engineer, Sterile and Liquids Pilot Plant

• Accountable for the generation of the global strategic V&I plan, its global and regional execution, and facilitating the rollout to the countries
• Aligns with Big Country Markets
• Captures market-specific needs and insights to inform global strategy, while also guiding local execution in alignment with global V&I plans
• Monitors external clinical trends and scientific developments through systematic insight collection from group input meetings (GIMs), congresses, and other platforms to maintain up-to-date knowledge of emerging science, medicines, and vaccines
• Leads the team in engagement with international scientific leaders and other key stakeholders about our company’s emerging science.

MSD