Manager

• This position leads the operational planning and execution of one or more clinical trials or significant aspects thereof.
• Responsible for the operational planning, feasibility, and execution of a clinical trial.
• May serve as the clinical trial team lead
• May lead team in key study planning, development, and execution elements (e.g., data management deliverables, trial level plans/timelines, country/site selection, site materials, system updates, investigator meeting planning, communication plans, preparation of status update reports, study close out activities).
• Leads team for timeline management, risk identification and mitigation, issue resolution.
• May facilitate and collaborate with key internal/external stakeholders (e.g., study team, country teams, vendors, committees) in support of clinical study objectives.
• Accountable for managing any study specific partners and/or vendors.

Senior Scientist, Study Manager

Marketing

• Collaborate closely with the Disease Asset Leads to develop and execute the Commercial strategy of late-stage hematology assets.
• Provide commercial leadership in close collaboration with Late-Stage Heme Asset Leads
• Drive innovative global execution to ensure critical launch deliverables are seamlessly adapted and deployed in priority markets, leveraging novel tools and approaches such as content accelerator and AI.
• Provide commercial leadership, where appropriate, into Scientific Strategy development & execution (e.g., Congress Planning, Scientific Platform development, Medical Education programs, Patient Engagement etc.)
• Collaboration with other functions /divisions in key markets to develop, plan and execute worldwide launches to ensure commercial and enterprise readiness.
• Collaboration with key markets to develop global strategy, 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.

Director, Global Oncology – Hematology

Software Engineer

• Lead integrated project teams to deliver critical assets on time and within budget
• Forecast and allocate internal and external resources to meet project workload
• Manage, mentor and provide ongoing feedback to direct reports including mid-year and annual reviews
• Develop close working relationships with Plant Managers, key staff, and stakeholders to align projects with business objectives and optimize value
• Approve and lead development of project execution plans and schedules that meet customer needs and reflect project risks
• Verify scopes provide least-cost, fit-for-purpose business solutions
• Manage project processes through effective design, execution strategies, and construction management oversight
• Implement and approve procurement strategies, contract administration, and project close-out activities
• Understand, set, and manage project cost budgeting, forecasting and control including approving spending forecasts using Target Value Delivery and Earned Value where applicable
• Manage schedule development and control to meet milestones and delivery targets
• Identify and rank project and process risks; develop and implement mitigation plans
• Act as a visible safety leader through project safety walks and peer safety reviews, promoting a zero-harm culture
• Manage project communications requirements, providing effective reporting and distribution of information to stakeholders.

Director, Engineering – Capital Projects

QA Engineer

• Perform GMP documentation review and approval for internal or outsourced manufacturing of clinical supplies including batch records, deviation and/or out-of-specification approval, change management approval, etc.
• Support the Quality Program Lead on inter-departmental and cross-functional teams, ensuring communication of accurate information and providing quality guidance and/or deliverables.
• Accountable for all assigned projects and communication of status to the Management team.
• Identify need for and/or develop SOPs to ensure practices are accurately reflected.
• Adhere to cGMPs and SOPs

Senior Specialist, Quality Assurance, Sterile Quality

Research Scientist

• Horizon scanning, developing, and managing strategic partnerships to accelerate and generate insights that inform healthcare decisions and policy through novel studies, methods, and technologies
• Managing collaborations and effectively identifying and communicating data needs and capabilities with extended stakeholders
• Leading knowledge management and data innovation initiatives to increase access to and interoperability of data, data strategy, models, analytics, and evidence
• Conducting data analytic projects using standard and advanced analytic methods to meet business objectives
• Partner effectively with Outcomes Research and Epidemiology teams to understand and address real-world data gaps and opportunities
• Maintaining awareness and communication of scientific and technologic developments within the fields of data science, informatics, and health technology assessment (HTA)
• Advancing, presenting, and publishing novel methodologies in the fields of data science and informatics at international/national congresses and in scientific and technology journals

Associate Principal Scientist – Real World Data Strategy, Partnerships

Content Marketing Manager

• Providing leadership, resources and direction to a group of professionals
• Overseeing the development and execution of the GSVC plans relevant to TAs
• Leading the incorporation of medical insights and feedback into the GSVC annual product plans
• Driving the effectiveness of the TA team through leadership
• Leading and/or commissioning the development of operational solutions and process improvements
• Directing and overseeing the daily tasks and operations of team members by providing guidance, assigning tasks, and ensuring productivity

Director, Team Lead – Global Scientific & Value Content, Infectious Diseases/Vaccines

Director

• Develop and co-own with Digital Manufacturing a multi-year digital and data strategy for biologics late-stage pipeline and inline aligned with enterprise priorities; translate strategy into a prioritized execution roadmap with clear business cases and ROI metrics.
• drive execution against that roadmap.
• Establish approach and drive acceleration of adoption of analytics, statistics, modeling, AI/ML and structured content practices in Bio S&T, while holding functions accountable for execution.
• This role will also be responsible for integrating across the Bio S&T functions in driving a robust knowledge management and document management strategy for CMC filings.
• This will be done in close integration and collaboration with Digital Manufacturing and Digital CMC.
• This role will oversee the integrated data architecture and governance model within Bio S&T that unifies process data across upstream/downstream, scale-up/tech transfer and commercial operations, including external CMOs/CDMOs.
• Serve as Bio S&T functional owner for key lab/process systems across Bio S&T (e.g ELN, utilization of VTN, KX etc); drive adoption and enable cross program learnings.
• Coordinate and sustain maintenance of process platforms and standards across Bio S&T functions, with functions holding content accountability.
• Identify needs, develop biologics tech business strategy for mechanistic/statistical modeling, predictive analytics, digital twins, and support NLP-enabled data extraction driving Bio S&T level execution of Digital CMC strategies, ensuring sustainability and efficiency.
• Drive strong collaboration with Digital Manufacturing to link business and data science & analytics capabilities in Digital Manufacturing.
• Define, track and report KPIs for data quality, model impact, process performance (yield, cycle time, first-pass success), submission timelines and cost savings, while driving execution through Bio S&T functions.
• Drive operationalization of analytics into workflows (experimental design, tech transfer, manufacturing control, lot release) and partner with continuous improvement teams to capture efficiencies.
• Integrate at site technology process data leads and above site process data leads driving to efficient and sustainable execution of overarching biologics data strategy and process monitoring.
• Oversee and streamline statistics support & training across Manufacturing process and analytical working groups, and functions.
• This role will partner very closely with Digital Manufacturing and Digital CMC to drive an integrated strategy for biologics across Bio S&T functions.
• This team will integrate existing local efforts on data management, data strategy, modeling, statistics, data sciences within Bio S&T.
• Drive change and adoption of data and digital mindset within Bio S&T across all functions and all levels of the organization.
• Recruit, develop and retain a multidisciplinary team; champion inclusive talent management and succession planning.

Executive Director, Bio S&T Platform, Data, Statistics & Modeling

Clinical Operations

• Provide oversight and leadership of clinical program execution
• Lead and direct global, cross-functional teams in end-to-end clinical development activities
• Responsible and accountable for the operational execution of a suite of clinical trials
• Lead and direct teams to support key program planning and execution elements
• Serve as the operational representative on the Product Development’s Clinical Subteam
• Contributes to resource planning and staffing (hiring and/or project onboarding, supervision of clinical scientists and study managers)
• Collaborate and facilitate interactions with key internal and external stakeholders
• Assist the Clinical Directors in scientific leadership/investigator initiatives
• May lead and/or implement process improvement and strategic initiatives

Principal Scientist, Clinical Operations – Immunology

Backend Engineer

• Accountable for the overall architectural integrity and strategic alignment of the Veeva platform across divisions
• Define and maintain enterprise Veeva platform architecture, principles, standards and guardrails
• Establish and lead the Veeva Community of Practice across divisions
• Drive cross-divisional alignment on platform strategy, ways of working, and priorities
• Align platform roadmap and OKRs with enterprise and divisional objectives
• Govern the Process Atlas as an enterprise dependency and prioritization mechanism
• Enable reuse, standardization, and continuous improvement across vault families

Veeva Platform Architect

Clinical Research

• Responsible for leading specific aspects of clinical/scientific execution of clinical protocol(s).
• Serving as the lead clinical scientist on the clinical trial team.
• Leading medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with the Clinical Director.
• Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents / amendments); Partners with the Study Manager on study deliverables.
• Ensuring CRF design supports data collection in alignment with the protocol in collaboration with Data Management/Programming.
• Collaborating cross-functionally to monitor clinical data to ensure quality, completeness, and integrity of trial conduct.
• Providing tactical/scientific mentorship to other clinical scientists.

Senior Clinical Scientist

• Translate deep knowledge of the Lung access landscape, competitors, payers and future access trends into access insights to develop access strategies
• Actively collaborate with the functions including but not limited to Oncology Global Market Access and Pricing Team, Oncology Global Marketing team, Oncology US Marketing, HH International, Global Pricing, Value and Implementation Teams, Policy, Regional Market Access teams, SAS, to provide critical lung market access viewpoints across stakeholder workstreams
• Work closely with the cross-functional teams to develop payer value proposition and scientific narrative that relates to pipeline assets with lung indications
• Lead the lung strategy development for selected pipeline assets in regard to their lung indications and lead discussions at selected key forums and meetings
• Monitor Oncology global competitors and comparator prices and strategy
• Collaborate with the GMAx asset leads on different aspects of the pipeline assets to ensure coherent strategy development

Director, Global Oncology Market Access – Lung

Project Manager

• Lead a portfolio of Pharma IT projects from initiation through closeout, including GxP systems (LIMS, ELN, clinical trial systems, manufacturing execution systems, data platforms), infrastructure, integrations, and digital transformation efforts.
• Define and enforce project governance, SDLC and validation-related processes, and reporting cadence; adapt and champion delivery methodologies (Agile, Waterfall, hybrid) appropriate to regulated environments.
• Develop comprehensive project plans, resource and capacity forecasts, risk and issue logs, dependency maps, and change-control processes aligned with quality and regulatory requirements.
• Oversee requirements management, vendor selection, contract execution, and third-party validation activities; coordinate with QA and validation teams to ensure compliance.
• Provide strong stakeholder engagement across R&D, Clinical, Manufacturing, Regulatory Affairs, Quality, IT Security, Data Governance, and Commercial functions; communicate status, risks, mitigation plans, and decision-ready options to senior leadership and steering committees.
• Manage financial aspects of projects: budget creation, tracking, variance analysis, and forecasting; ensure cost controls and value realization.
• Mentor, coach, and develop project managers and technical leads; establish clear performance expectations and career development plans.
• Lead risk management and contingency planning, including cybersecurity risk assessments and business continuity considerations for critical systems.
• Drive continuous improvement in project delivery, including lessons learned, metrics, and process optimization tied to compliance and quality outcomes.
• Facilitate regulatory readiness activities and audit support, prepare project artifacts for inspections, and ensure traceability of requirements, design, testing, and release records.

Associate Director – Technical Project Management

• Develop professional relationships with scientific leaders to share medical information
• Conduct peer-to-peer scientific discussions
• Support Company-Sponsored Trials and enhance understanding of scientific foundations
• Initiate discussions with potential investigators
• Recommend potential study sites

Oncology Regional Medical Scientific Director – Genitourinary Oncology

• Translate patient, caregiver, and market insights into clear opportunities that shape patient marketing strategy, messaging, and experience design.
• Define research objectives and oversee qualitative and quantitative studies to understand patient needs, barriers, motivations, and journey dynamics.
• Partner with analytics, digital, and marketing teams to build measurement frameworks that evaluate full-funnel performance across DTC and patient engagement channels.
• Develop and maintain dashboards, reporting structures, and KPIs that provide visibility into campaign effectiveness and consumer behavior trends.
• Identify performance optimizations and recommend data-driven enhancements to targeting, messaging, channel mix, and journey design to improve patient acquisition and conversion.
• Support test-and-learn agendas by designing hypotheses, creating experimentation plans, and analyzing outcomes to inform future marketing strategies.
• Collaborate with cross-functional partners, including brand, media, digital, CRM, market research, analytics, and agency teams, to ensure insights and data are embedded throughout planning and execution.
• Synthesize complex data into clear, compelling narratives and recommendations for senior leadership and key stakeholders.
• Monitor competitive trends, category dynamics, and shifts in patient expectations to inform proactive strategy adjustments.
• Ensure all insight generation, data usage, and analytic practices adhere to compliance, privacy, and regulatory guidelines.

Associate Director, U.S. Marketing – HCC Insights, Data & Optimization

Financial Planning and Analysis

• Oversee the forecast process related to Translational Medicine studies, as well as providing financial support for associated collaborations with external partners across the General & Specialty Medicine, Vaccines and Infectious Diseases therapeutic areas.
• Work across the CDF team to provide financial reporting and analytical support in order to enhance business insights for our Research Department business partners.
• Lead a team of finance professionals serving as point of contact for multiple stakeholders including external partners, Global Project and Alliance Management, Early Development Team (EDT) Leaders, Product Development Team (PDT) Leaders, and Clinical Study Managers regarding study budgets, site and vendor related payments
• Partner with Discovery, Preclinical, Translational Medicine (DPTM) Finance to monitor progression of preclinical candidates (PCC) and assess financial impacts of PCC conversion to clinical compounds
• Develop and participate in team presentations to the Discovery and Translational Research Committee (DTRC) and the Late Development Review Committee (LDRC).
• Support project team decision making by providing relevant financial information and insight
• Own critical components of the Long Range Operating Plan (LROP), Budget, and Quarterly Forecasts
• Confirm accurate accounting of all US site payments related to visits completed, milestones completed and reimbursement for out of pocket expenses according to Generally Accepted Accounting Principles, the Sarbanes Oxley Act as well as internal and external accounting guidance

MSD