Research Scientist

• Lead early clinical development strategy for novel therapy programs from Preclinical Candidate approval through Phase 1 and Phase 2 clinical Proof-of-Concept
• Develop biomarker strategies through cross-functional teams from First-in-Human studies through clinical Proof-of-Concept
• Conduct Experimental Medicine studies to establish or validate biomarker platforms
• Partner with discovery research teams to contribute a clinical perspective to target identification and validation
• Execute clinical studies evaluating potential targets and their relevance to human disease
• Develop and execute clinical pharmacology strategies from Phase 2 through worldwide marketing application
• Provide leadership as a key member of early development teams
• Author clinical and biomarker plans for Lead Optimization programs, Preclinical Candidate molecules, and Phase I–IV clinical pharmacology studies
• Develop and execute studies validating clinical platforms using imaging, electrophysiological, and behavioral biomarkers
• Design preclinical and/or clinical pharmacology experiments to validate targets and pathways
• Safely and timely execute Phase I studies
• Collaborate with internal and external clinical study support staff and scientists across discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs, and global clinical trials operations
• Provide clinical pharmacology support through worldwide marketing application filing, including registration documents and presentations
• Communicate and interpret study results to therapeutic area governance, functional area experts, and development review committees
• Assess internal and external opportunities identified by Business Development and Licensing
• Interface with Discovery Sciences, Preclinical Pharmacology, Pharmaceutical Sciences, Toxicology, Translational Biomarkers, Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs, and late-stage Clinical Research teams worldwide

Principal Scientist – Translational Medicine, Cardiovascular

• Provide strategic and scientific biomarker leadership across Cardiovascular & Metabolic and Infectious Diseases/Vaccines portfolios
• Lead design, execution, analysis, and communication of translational and clinical biomarker strategies from early through late clinical development
• Develop decision-centric biomarker strategies integrating therapeutic mechanism, disease biology, pharmacodynamics, patient heterogeneity, dose and regimen selection, clinical endpoints, and precision medicine opportunities
• Develop and lead integrated biomarker strategies with cross-functional development teams
• Translate disease biology and therapeutic mechanism into translational hypotheses and fit-for-purpose biomarker approaches
• Define biomarker contributions to proof of biology, target engagement, dose and regimen selection, patient stratification, response assessment, and go/no-go decisions
• Serve as biomarker representative on cross-functional program teams
• Partner with Discovery, Clinical Development, Quantitative Sciences, Regulatory, Data Science, Clinical Operations, and other functions
• Lead interpretation of biomarker and clinical datasets and translate findings into actionable recommendations
• Identify disease heterogeneity, therapeutic response, resistance or non-response, and biological drivers of clinical outcomes
• Develop infectious disease and vaccine biomarker strategies addressing host and pathogen biology, immune response, correlates of protection, pharmacodynamic response, and stratification
• Develop cardiovascular and metabolic biomarker strategies addressing target engagement, pathway modulation, disease biology, pharmacodynamic response, patient heterogeneity, and biological/clinical outcome relationships
• Evaluate emerging biomarker technologies and analytical approaches
• Communicate strategies, results, risks, and recommendations to stakeholders
• Provide scientific guidance and mentorship to biomarker scientists
• Support publications, scientific presentations, external collaborations, and interactions with external experts

Principal Scientist, Translational Clinical Biomarkers

Medical Director

• Manage scientific knowledge and provide strategic, medical, and scientific guidance for upcoming oncology indications, including solid and hematologic malignancies
• Develop, prioritize, and execute strategic and tactical Oncology Medical Affairs plans
• Identify medical and scientific gaps and prioritize tactics to address the needs of clinical scientific leaders
• Serve as the national point of contact for the regional Medical Affairs team
• Collaborate with global and regional teams to secure support for Canadian projects
• Support Phase II and III studies, local clinical evaluations, and investigator-initiated studies
• Encourage the conduct of clinical development studies in Canada
• Act as the medical point of contact for Market Access, Health Economics and Outcomes Research, Clinical Research, Marketing, and Regulatory Affairs
• Support the management of existing products and the launch of new products
• Participate in cross-functional brand teams and provide scientific expertise
• Support product approval submissions and the preparation of regulatory reports
• Establish professional relationships with key scientific leaders in Canada, regulatory agencies, payer groups, and patient advocacy organizations
• Share medical and scientific expertise with Regulatory Affairs, R&D, Quality Assurance, Legal, and Marketing teams

Associate Director (Medical Advisor), Oncology – Pipeline & Hematology

Financial Planning and Analysis

• Lead a team of 2 Associate Directors providing compliance support to the US Market Finance team
• Ensure all aspects of the US Market Finance Compliance Plan are met
• Facilitate the annual SOX audit with internal and external auditors
• Coordinate annual reviews and training on internal controls, standard operating procedures, work instructions, and government pricing policies
• Prepare quarterly State of Compliance reports and conduct compliance reviews with US Market Finance and Compliance senior leaders
• Manage the quarterly control process and ensure significant matters are identified and evaluated promptly
• Provide compliance subject matter expertise on commercial initiatives through cross-functional team participation
• Advise on implementation of new projects, systems, and processes to ensure financial data integrity and compliance with SOX and other financial requirements
• Identify, investigate, and implement preventative actions for remediation items
• Communicate the importance of compliance throughout the organization
• Report directly to the US Finance Lead and via dotted line to the Human Health US Compliance Lead

Director, Financial Processes & Control

Clinical Research

• Strategically plan and direct clinical research activities involving investigational compounds in Immunology
• Manage the full clinical development cycle, including indication selection, study design, initiation, execution, monitoring, analysis, regulatory filing, and publication
• Evaluate pre-clinical and translational work to generate early clinical development plans and Investigational New Drug applications
• Support business development assessments of external opportunities to grow the Immunology pipeline
• Develop clinical development strategies and plan clinical trials
• Monitor and manage ongoing and new clinical trials
• Analyze and summarize clinical findings to support safety and efficacy decisions, new drug applications, clinical study reports, and publications
• Participate in internal and joint internal/external research project teams
• Supervise Clinical Scientists executing clinical studies
• Collaborate with commercialization, regulatory affairs, statistics, and manufacturing experts
• Keep corporate personnel informed about study progress, competitor drugs, and relevant scientific questions
• Maintain scientific knowledge and identify strong investigators
• Establish collaborations with external experts in rheumatologic diseases
• Attend scientific meetings
• Author development documents, presentations, budgets, and position papers
• Facilitate collaborations with external researchers worldwide
• Travel on company business to manage clinical research projects

Principal Scientist, Clinical Research, Immunology

Inside Sales

• Interact virtually with customers and understand their needs
• Consult customers on solutions within Canine and Feline product portfolios
• Work with veterinary clinics, shelter facilities, and corporate accounts in the assigned territory
• Sell Animal Health division products and support pull-through activities
• Serve as the primary contact for assigned customers and connect with decision-makers
• Develop customer strategies, territory plans, and key account plans
• Partner with National Account Managers, Corporate Account Team, and Distribution Partners
• Collaborate across species teams to promote the full Animal Health product portfolio
• Analyze monthly sales results and manage expenses within budget guidelines
• Identify programs and services to address customer needs and provide education and training
• Work with leadership and Professional Services to develop and deliver relevant offerings
• Maintain knowledge of products, industry trends, competitors, and omni-channel demand generation tools
• Communicate customer, industry, product, and market trends through the organization
• Meet learning and development objectives agreed upon with leadership

Inside Sales Account Representative

Full-stack Engineer

• Build engineering capabilities related to medical devices and combination products
• Manage internal and external manufacturing through development, scale-up, commercialization, and design transfer
• Support complex drug-delivery systems including autoinjectors, ophthalmic products, and inhalation products
• Serve as a technical subject matter expert on device components, combination products, and processes
• Support global commercialization and technology transfer activities
• Drive product robustness for sustained launch while maintaining quality and regulatory compliance
• Develop solutions using design controls, design transfer, control strategies, device risk management, and design verification testing
• Support internal and external component and combination product manufacturing globally
• Identify issues, determine root causes, and provide solutions
• Optimize design and manufacturing using engineering best practices and tools
• Support regulatory agency responses and pre-approval inspections
• Develop and execute technology-transfer and problem-solving plans
• Lead teams in late development stages and collaborate with internal and external partners
• Build strategic partnerships with manufacturing sites and partner groups
• Support regulatory inspections and maintain compliance with quality management systems

Senior Engineer, Device Technical Operations

Director

• Lead and shape quantitative pharmacology strategy across oncology programs to inform dose selection, trial design, and go/no-go decisions
• Develop and implement integrated model-informed drug development (MIDD) strategies across development stages
• Align modeling strategies with regulatory expectations and business priorities
• Maintain understanding of global regulatory expectations for small molecules, biologics, ADCs, and TCEs
• Lead, mentor, and develop a team of QP2 scientists, including performance management, hiring, retention, and talent development
• Provide scientific and operational oversight to ensure high-quality and timely deliverables
• Contribute to QP2 and Oncology leadership initiatives, talent strategies, and organizational priorities
• Support resource planning and allocation with senior leadership
• Serve as QP2 lead on assigned programs and represent QP2 in cross-functional teams and governance forums
• Collaborate with Translational, Clinical, and Biostatistics teams to integrate quantitative insights into development strategies
• Partner with preclinical teams to translate nonclinical findings into clinical development plans
• Contribute to due diligence for business development and licensing opportunities
• Develop and contribute to regulatory strategies and author or review INDs, CSRs, CTD modules, and NDA/BLA submissions
• Ensure high-quality clinical pharmacology and pharmacometric analyses and reports
• Represent the company in regulatory agency interactions, scientific conferences, and external collaborations
• Report directly to the QP2 Oncology Executive Director

Group Leader – Senior Director, Quantitative Pharmacology and Pharmacometrics – Oncology

• Serve as an expert representative for QP2-IO on Oncology clinical development teams
• Frame critical questions for optimizing model-based analyses on programs
• Develop and execute model-based analyses, including translational PK/PD approaches, population pharmacokinetic models, exposure-response models, clinical trial simulation, disease progression models, QSP modeling, and comparator modeling
• Strategize and execute modeling of tumor size and survival endpoints, including proportional hazards models
• Maintain comprehensive understanding of global regulatory expectations for small molecules and biologics in Oncology
• Author regulatory documents, including INDs, CSRs, and CTAs/CTDs
• Represent QP2-IO at regulatory meetings
• Collaborate with QP2-IO, cross-functional teams, external vendors, and partners to support drug development strategies and decisions

Associate Director, Quantitative Pharmacology and Pharmacometrics – Immuno-Oncology

Software Engineer

• Shape and advance the agentic intelligence agenda for DSCS Digital Operations
• Identify where agents, data products, and automation create the greatest business value
• Translate priorities into a sequenced roadmap
• Own projects and programs through design, build, evaluation, deployment, adoption, and sustainment
• Exercise independent technical and business judgment on what to build, standardize, retire, or decline
• Translate complex business challenges into technical roadmaps, solution designs, agent architectures, evaluation frameworks, and measurable outcomes
• Establish engineering and governance standards, including version control, documentation, testing, reusable patterns, and release-readiness controls
• Lead teams and projects and coach talent across multiple technical areas
• Partner with business leaders to drive adoption and demonstrate value realization
• Direct the design, delivery, and lifecycle governance of intelligent agents and AI-enabled workflows
• Set direction for data pipelines, semantic layers, and reusable data products
• Oversee dashboards, applications, and workflow automations
• Define reference architectures and integration patterns and lead design reviews
• Align solutions to decision frameworks, KPIs, and adoption measures
• Establish evaluation and testing standards for agents, data, and reporting solutions
• Establish source control, code review, automated testing, CI/CD, and gated release promotion practices
• Set standards for design documents, runbooks, decision logs, and handover materials
• Own production sustainment, performance monitoring, issue triage, user support, and retirement or rework
• Partner with IT, cybersecurity, privacy, quality, and data product owners on security, compliance, and governance
• Mentor engineers and analysts and raise technical capability through coaching, code review, and shared learning
• Evaluate emerging models, platforms, and agentic patterns and recommend adoption, piloting, or deferral

Associate Director, Engineering

Chief Marketing Officer

• Lead LROP and Profit Plan efforts for sac-TMT across tumors
• Drive planning, monitoring, and launch success across the team
• Align global guidance and forecasts for sac-TMT with strategic forecasting and sac-TMT marketing teams
• Coordinate forecasting and partnership with strategic forecasting, finance, and DDA colleagues
• Build trusted partnerships with disease, asset, functional, regional, and market-based counterparts
• Lead sac-TMT brand-direction forecasting efforts across indications for twice-yearly forecasts, Overlay, Profit Plan, and additional forecasts
• Serve as point of contact with the forecasting team for new study forecasts during leadership reviews and prioritization gap analysis
• Lead Trimester business reviews for sac-TMT
• Establish and standardize post-launch performance reporting across indications with DD&A
• Serve as new product leader for long-term registrational clinical trials and signal-finding studies
• Evaluate new sac-TMT opportunities to address unmet patient needs in consultation with asset, tumor marketing, clinical, and medical colleagues
• Advance global marketing and alignment across stakeholders for current and future indications

Director, Global Marketing

• Develop AI-ready data foundations, semantic data layers, data pipelines, dashboards, web applications, automations, and intelligent agents for DSCS digital operations
• Design, build, test, document, and provide operational support for governed data products, reporting solutions, automations, and intelligent agents
• Translate business needs into technical requirements, data requirements, agent instructions, test cases, and acceptance criteria
• Apply Git-based version control, documentation, testing, reusable templates, and release-readiness checks
• Collaborate with business, data, technology, quality, and compliance stakeholders
• Support governed agents and AI-enabled workflows using Copilot Studio, Gemini/Vertex AI or comparable platforms, Microsoft Power Platform, APIs, connectors, and approved data sources
• Contribute to agent lifecycle activities including intake, proof of concept, MVP readiness, deployment validation, sustainment, monitoring, and retirement
• Build and maintain data pipelines, curated datasets, semantic layers, and reusable data products using Python, SQL, Databricks, Dataverse, Power BI, SharePoint, and other approved platforms
• Develop and maintain dashboards, reports, web applications, Power Apps, Power Automate flows, and workflow automations
• Create and execute test cases for agents, automations, data pipelines, and reports
• Evaluate response quality, grounding accuracy, task success, failure modes, regression performance, monitoring needs, access controls, and responsible deployment requirements
• Use GitHub, VS Code, branching, pull requests, code review, reusable templates, design notes, runbooks, decision logs, and handover materials

Engineering Specialist

Representative

• Interact face to face with veterinary clinic, shelter facility, and corporate account customers
• Understand and identify customer needs and sell the Animal Health division’s Companion Animal product portfolio
• Support pull-through activities aligned with customer strategy
• Serve as primary point of contact for assigned customers and meet with key personnel and decision-makers
• Develop customer strategies, territory plans, and account plans
• Partner with National Account Managers, Corporate Account Team, and Distribution Field Partners
• Collaborate across species teams to promote knowledge of the Animal Health product portfolio
• Share with regional team members to support growth and development
• Analyze monthly sales results and manage expenses within budget guidelines
• Identify programs and services to address customer needs and provide education and training opportunities
• Work with leadership and Field Professional Services to develop and deliver relevant offerings
• Maintain knowledge of Animal Health products, industry trends, and competitors
• Communicate customer, industry, product, and market trends throughout the organization
• Develop and meet learning and development objectives agreed with leadership

Senior Territory Representative, Companion Animal

Procurement

• Develop and deliver global procurement and category strategies across direct materials, indirect services and capital investment
• Lead strategic sourcing, complex negotiations, contract management and supplier governance
• Build partnerships with senior business leaders and provide market, supplier and commercial insights for business decisions and investment planning
• Manage supplier performance, third-party risk, due diligence, business continuity and compliance across global operations and supply chains
• Lead, coach and develop a global procurement team of approximately six procurement professionals
• Advance procurement capabilities through process improvement, digital tools, data-informed decision-making and support for business transformation and integration activities
• Partner with leaders across manufacturing, supply chain, research and development, commercial operations, finance, quality, regulatory affairs, engineering and technology

MSD