Compliance

• Provides administrative support during filling and review of new product registrations and post-approval submissions
• Plan and coordinate regulatory submissions to ensure timely delivery
• Draft and organize regional administrative documents and liaise with internal teams for completeness and accuracy
• Work closely with Regulatory Operations and Country RA Managers to establish submission timelines and align on submission strategy and execution
• Oversee translation processes to meet EMA requirements
• Coordinates new product artwork development and/or artwork updates implementation
• Keep regulatory databases updated and ensure adherence to EU legislation and procedural requirements
• Act as a subject matter expert in workstreams and process improvement initiatives

Associate Liaison, Regulatory Affairs – Europe

Research Scientist

• Provide medical and scientific leadership in the use of clinical imaging in clinical development.
• Interface with internal stakeholders and external collaborators (such as imaging service vendors).
• Design and oversee existing imaging strategies for early and late-stage clinical trial support.
• Exercise foresight and judgment in planning, organizing, and guiding complex imaging projects.
• Work across departments to advance imaging processes.
• Work with quality and compliance teams for quality-related decision making internally, and assist with vendor audits as needed.
• Identify needs and lead internal initiatives and collaborations, with a focus on scientific innovation to advance the application of imaging.

Imaging Lead – Senior Principal Scientist

Marketing

• Own and refine the HCP GI strategy (upper and lower) across customer segments to maximize commercial performance of the GI portfolio and align field and non-field tactics to drive business priorities
• Translate customer segmentation insights into targeted personal and non-personal promotional plans that positively impact the business
• Lead cross-functional workstreams to monitor business performance, diagnose growth opportunities, and execute data-driven plans in partnership with digital analytics, competitive intelligence, and market research
• Serve as a decisive project lead: define clear goals and success metrics, prioritize initiatives, manage complex timelines and resources, proactively identify and mitigate risks, and escalate issues to preserve momentum and deliverables
• Direct the end-to-end development and execution of HCP promotional materials — including digital channels and omnichannel tactics — ensuring scientific accuracy, regulatory compliance, and commercial effectiveness
• 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
• Collaborate closely with market access team to identify payer trends, translating those insights into tactical adjustments and strategic recommendations for the GI Cancers business
• Partner 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
• Lead GI scientific strategy and embed scientific insights into HCP strategy, congress', assets, and training
• Coordinate with Medical Affairs, CI, and Publications to translate post-congress insights for commercial execution
• Manage the GI Cancers and Melanoma budget

Associate Director – US Oncology – GI Cancer HCP Strategy & Execution Lead

Director

• Lead and oversee label translation coordination activities including intake, tracking, prioritization and completion of translation requests.
• Lead and oversee label documentation control activities including label generation, review/approval of vendor label proofs, randomization and variable text reports.
• Provide leadership, direction and coaching to team members responsible for translation and document control activities.
• Coordinate with cross-functional stakeholders to support business priorities, timelines and operational needs.
• Monitor workload, performance and resources to ensure operational and compliance expectations are achieved.
• Identify process gaps, delays or risks and implement or recommend corrective actions.
• Support audit readiness by ensuring documentation is current, organized and inspection ready.
• Contribute to process improvement initiatives to enhance efficiency, consistency and quality.

Associate Director, Planning & Scheduling

Software Engineer

• Lead the strategic direction and overall performance of Central Utilities systems which include, chilled water, cooling tower systems, plant air, and related infrastructure, ensuring safe, compliant, and reliable operations
• Serve as the site’s subject matter expert for central utility systems, advising operations, maintenance, and capital project teams on system design, reliability, and regulatory compliance
• Manage and mentor the central utilities group, providing guidance on operational practices, technical expertise, and team development
• Collaborate with cross-functional teams, including project management, real estate, facility management, and master planning to ensure seamless integration of central utility systems with organizational goals and initiatives
• Develop and implement policies, procedures, and best practices for operations and maintenance, ensuring compliance with EPA refrigerant standards and other relevant regulations
• Oversee budget planning and resource allocation for central utilities related projects, ensuring projects are completed on time and within budget constraints
• Drive initiatives for energy efficiency and sustainability within utility operations to align with the company’s commitment to environmental stewardship
• Accountable for refrigerant air emissions compliance
• Serve as the primary point of contact for external audits, inspections, and regulatory compliance related to central utility systems

Associate Director, Engineering Central Utilities

• support statistical programming activities for multiple and/or large/complex late-stage drug/vaccine clinical development projects
• development and execution of statistical analysis and reporting deliverables
• design and maintenance of statistical databases
• key collaborator with statistics and other project stakeholders
• assure deliverable quality and process compliance
• maintain and manage a project plan including resource forecasting
• coordinate activities of a global programming team
• membership on departmental strategic initiative project teams

Associate Principal Scientist, Statistical Programming, Late-Stage

Medical Director

• Planning clinical trials (designing, collaborating on operational plans, etc.) based on the clinical development strategy.
• Medical oversight and overall conduct of ongoing or new clinical trials for investigational or marketed drugs.
• Analyzing and summarizing clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication.
• Supporting business development assessments of external opportunities.

Clinical Director, Clinical Research, Hematology

DevOps Engineer

• Build relationships across the broader IT organization to increase adoption and maturity of SRE, Observability, and Resilience practices
• Define and evolve the strategic vision for enterprise reliability engineering and ensure alignment across product, platform, and ITSM teams
• Establish and enforce standards for Service Level Objectives, observability frameworks, and resilience engineering practices
• Collaborate with engineering teams to ensure reliability is embedded into architecture, design, and delivery processes
• Drive adoption of Service Level Objectives using Nobl9 as the system of record for reliability governance
• Lead evaluation and introduction of new technologies that improve reliability outcomes while integrating with existing platforms
• Apply AI capabilities to enhance reliability practices, including incident triage, diagnostics, and automation, in a governed and controlled manner
• Collaborate within efforts to standardize observability across logs, metrics, traces, and events to improve system visibility and decision-making
• Consult and promote resilience patterns including fault isolation, failover strategies, and recovery mechanisms
• Guide improvements surrounding incident lifecycle effectiveness, including detection, response, root cause analysis, and continuous improvement
• Lead and mentor a community of reliability practitioners to grow organizational capability and maturity
• Represent reliability engineering practice in architecture reviews, governance forums, and key IT initiatives
• Drive continuous improvement of reliability practices through research, innovation, and feedback from engineering teams

Senior Staff Reliability Engineer, Software Engineering

• Leading the commercial strategy development for the sac-TMT launch indications in Breast, with a focus on TF-10 and TF-11 trials, including driving the development of indication-level L3 marketing strategy deliverables, scientific narrative, nurse/care team strategies, in close collaboration with relevant disease teams, ensuring consistency and cohesion with the overarching sac-TMT asset strategy and relevant disease portfolio strategies
• Includes responsibilities for market research, SL insights and other related insight-gathering needs for initial launch indications
• Includes coordination with precision medicine team on biomarker strategies related to initial launch indications
• Leading commercial planning and execution for the initial launch indications for sac-TMT, including: Development of promotional strategies, messaging and any necessary global content deliverables, in collaboration with relevant disease, cross functional and regional teams, and ensuring consistency and cohesion with the overarching sac-TMT asset strategy and relevant disease portfolio strategies
• AOR oversight and management
• Management of the launch planning process for sac-TMT in breast, ensuring close cross-functional and cross-geographic coordination
• SL engagement/congress strategy for initial launch indications, in coordination with relevant disease teams and broader sac-TMT asset planning workstreams
• Data analytics, performance metrics tracking for initial launch indications, in close coordination with relevant disease teams and sac-TMT analytics team
• Coordination with precision medicine team on BMx strategy scenario plans
• Leading the launch GCT for sac-TMT for Breast indications
• Preparation for launch readiness and other governance discussions related to the initial launches of sac-TMT

Director, Global Oncology – Breast Cancer

• The Executive Director has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs for oncology indications.
• The Executive Director will manage and oversee the entire cycle of clinical development, including study design, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation at national and international meeting.
• They will provide internal scientific leadership for cross-functional areas supporting clinical trials and will interact externally with key opinion leaders.
• 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 that incorporate the latest scientific developments, regulatory requirements, the competitive landscape, and commercial considerations
• Planning clinical trials (design, operational plans, settings) based on these clinical development strategies
• Monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed vaccines
• Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication
• Participation in internal and joint internal/ external research project teams relevant to the development of new compounds, and the further study of marketed compounds and support of business development assessments of external opportunities.
• The Executive Director may manage other Directors and/or Senior Directors responsible for oncology clinical development programs or projects.
• Mentoring and career development for direct reports (when applicable) will be a key function of the role.
• Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Vice President in ensuring that appropriate corporate personnel is informed of the progress of studies of our company and competitors' drugs and internal and external expert opinion on scientific questions relevant to their areas of responsibility.
• The Executive Director is responsible for maintaining a strong scientific fund of knowledge by:
• Maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies
• Identification of scientifically and operationally strong investigators who can assist in the development of our company's investigational and marketed drugs
• Establishing communications with prominent clinical investigators in their particular field of interest, particularly those who will be willing and able to assist in the evaluation of our company's drugs
• Attending appropriate scientific meetings to maintain their competency and to maintain awareness of research activities in their area of responsibility.
• Travel on company business about twenty (20) percent of the time to manage future or ongoing clinical research projects.

Distinguished Scientist – Asset Development Team Leader

Accounting Manager

• Manage daily AR operations: invoice validation, posting, cash application, account reconciliations, and aging management for assigned portfolio
• Lead collections activities: prioritize overdue accounts, conduct collection calls, negotiate payment arrangements, and escalate high-risk situations
• Investigate and resolve billing disputes, deductions, and misapplied payments; collaborate with Billing, Commercial, and Customer Service to close issues quickly
• Prepare and present AR metrics and trends (DSO, aging, dispute aging) and provide analysis to stakeholders
• Support month-end and quarter-end close tasks including AR reconciliations, journal entries, and variance analysis
• Maintain customer master data, payment terms, and invoicing preferences to ensure data integrity across systems
• Drive process improvement and automation initiatives to increase efficiency and reduce errors (e.g., lockbox, e-invoicing, AR workflow tools)
• Act as escalation point and mentor for junior AR staff; support audits and ensure compliance with internal controls

Specialist, Shared Services Accounting

Content Marketing Manager

• Own and maintain country-specific HR knowledge content, ensuring alignment with global HR standards
• Create, review, approve, publish, and retire HR knowledge articles
• Coordinate timely updates to knowledge content following policy changes, regulatory updates, audit findings, or process changes
• Serve as a key HR contact for knowledge content related to HR policies, procedures, translations & AI Readiness Guidelines
• Perform regular knowledge audits and health checks to validate accuracy, compliance, and completeness of country-level HR content

HR Content Compliance Specialist

• Own and evolve the global HR knowledge content strategy aligned to AI-enabled HR service delivery and enterprise governance standards.
• Define and enforce content governance frameworks, including roles, ownership, review cycles, approvals, and retirement processes.
• Establish clear standards for content structure, taxonomy, metadata, and lifecycle management to ensure consistency across regions and HR domains.
• Ensure HR knowledge content is structured, simplified, and optimized for AI consumption, including conversational AI, digital assistants, and agentic workflows.
• Partner with AI, digital HR, and platform teams to improve AI response accuracy, relevance, and confidence through content optimization.
• Translate complex HR policies and processes into plain-language, employee-centric content that AI can reliably interpret and surface.
• Lead global content audits and assessments using defined quality and AI-readiness frameworks (e.g., clarity, accuracy, structure, metadata completeness).
• Identify duplication, gaps, and outdated content; drive consolidation and remediation efforts across HR knowledge repositories.
• Establish content health metrics and scorecards to measure effectiveness, usage, user satisfaction and AI performance impacts.
• Partner with HR Enterprise Services, HR Solutions, Compliance, Regional HR Service Delivery teams as well as cross-functionally (IT & Finance) to ensure globally consistent yet locally relevant knowledge content where applicable.
• Enable and coach distributed content owners and SMEs on AI-first content design principles, templates, and standards.
• Act as the central point of coordination for translation compliance, localization, and global rollout/governance of HR knowledge updates.
• Serve as the knowledge content lead working with HR knowledge platform owners for related systems (e.g., ServiceNow Knowledge, Ask HR).
• Collaborate with platform owners & HR Solutions to align content design with system capabilities and AI roadmaps.
• Support pilots and launches of new AI-driven HR experiences by ensuring content readiness and sustainability.

Global HR Content Senior Specialist

Account Manager

• Lead strategic key account management and go direct business growth for all Indonesia
• Drive commercial performance, develop long-term partnership and ensure profitable
• Create 3 yrs strategic plan in key account, market entry strategy and Portfolio prioritization
• Achieve market share growth in Go direct segmentation, strong relationship and create business review with key account by quarterly
• Take full accountability for revenue, costs and profitability
• Implement structured performance management and KPIs to ensure consistent execution and results
• Lead and develop people to deliver results and grow together as team

Strategic Key Account Manager – Animal Health

• Coordinate the preparation, review, and submission of regulatory dossiers for new product registrations and post-approval submissions in the EU, UK, Switzerland, and non-EU SEE countries.
• Work with cross-functional project teams to develop and implement regulatory strategies, including scientific advice, pediatric investigational plans, and orphan designation.
• Identify regulatory risks and ensure alignment of regulatory strategies with project teams and business objectives.
• Accountable for interacting with regulatory agencies and Country RA teams to facilitate smooth submission, assessment, and quick approval of CTAs under the EU Clinical Trial Regulation.
• Serve as the primary regulatory representative to regulatory agencies and Country RA teams.
• Act as the Regulatory Affairs representative on assigned non-product related cross-functional teams.
• Develop and implement effective processes to meet business objectives and ensure compliance with regulatory requirements.
• Continuously build and maintain a sound scientific knowledge and expertise in assigned product areas and regulations.

MSD