Product Designer

• Serve as the primary Global learning consultant for assigned Brands/Franchise, establishing and sustaining strong relationships with brand, sales, and functional leaders
• Consult with stakeholders to identify performance needs, capability gaps, and desired business outcomes aligned to brand and launch strategies
• Translate business and performance into an integrated learning strategy that may include training and non-training solutions
• Monitor trends, data, and feedback to continuously refine learning strategies and recommend improvements
• Report on learning initiative progress, risks, and key decisions in regular business forums, including high-stakes cross-functional leadership meetings
• Design scalable, learner-centric, science-based learning journeys by persona and role, aligned to global learning and brand strategy
• Create high-level designs, detailed design documents, learning blueprints, and content frameworks across multiple modalities (digital, virtual, ILT, blended)
• Partner closely with Learning Developers, SMEs, and vendors to ensure fidelity to design intent and business outcomes
• Oversee internal and external vendors responsible for learning design and development, ensuring quality, scalability, speed, and cost-effectiveness
• Manage learning programs end-to-end, including timelines, dependencies, prioritization, and stakeholder communication
• Anticipate commercial reviewer concerns by proactively preventing claim creep and tone risks, ensuring fair balance framing while maintaining appropriate scientific depth for the defined learner persona
• Support training delivery and/or enable subject matter experts and trainers as needed for Global markets
• Analyze learning effectiveness data, learner feedback, and business impact metrics

Senior Specialist, Therapeutic Excellence Learning Experience Designer

Product Manager

• Ensure Live Archiving solutions implemented are consistent with our company’s evolving Data Governance strategy and direction
• Create trusted relationships with stakeholders, development team and users to help shape and drive the product vision
• Continuously discover and prioritize the best opportunities to deliver business value and meet the needs of our users
• Champion the product, driving excitement and support in a domain typically resistant to change
• Author, prioritize and manage the product roadmap and backlog in partnership with process owners, the development team and key stakeholders
• Dive deep into the compliance domain to understand the business priorities and user needs
• Partner with the development team to understand technology constraints and opportunities
• Leverage user feedback and product metrics to enable data-driven decisions
• Manage project escalations, issues, risks and dependencies

Product Owner, Active Data Management

Director

• Lead the end-to-end development and strategic positioning of Section I, one of the most critical elements of our IRA submission, ensuring alignment across V&I, Medical, and IAM while shaping the narrative for external review
• Interpret and evaluate evolving program guidance as the price negotiation initiative matures, and translate implications into strategic recommendations to our long-term strategy and forecast
• Serve as the policy team liaison to lifecycle management workstreams occurring across the US and Global commercial teams
• Ensure consistent awareness, understanding, and application of IRA assumptions to inform scenario plans and financial modeling exercises
• Lead responses to state PDAB affordability reviews of our Company's Oncology products, in partnership with Policy and V&I
• Work with IAM team to develop PDAB Playbook to ensure consistent thinking and response to state affordability reviews
• Evaluate potential upper payment limit (UPL) scenarios and drive cross-functional alignment on mitigation strategies
• Monitor landscape trends and performance data across identified top accounts to assess impact to business
• Analyze 340B policy and market evolution, including contract pharmacy dynamics, site-of-care shifts, and potential rebate models to assess business impact and inform strategic response
• Partner with cross-functional stakeholders to align enterprise perspectives and integrate 340B considerations into broader access and pricing strategies
• Partner with OCAR New Products team to assess impact of 340B evolutions to future strategy for pipeline assets
• Bring policy updates to the broader organization to build understanding of potential implications to the business over time

Associate Director, US Oncology Access Policy

Software Engineer

• Lead, mentor, and develop a team of technical staff, fostering a culture of continuous improvement.
• Provide subject matter expertise and ensure scientific rigor, technical problem solving, and execution excellence across the portfolio.
• Provide strategic leadership and direction for the development of standard work to characterize the real-world distribution environment.
• Ensure thorough engineering and distribution packaging science is applied to deliverables for new product introductions and technology transfers across the network.
• Deliver the development, design, construction, qualification/validation, and/or initial operation of complex tertiary packaging components and processes.
• Drive proactive risk management activities, including risk assessment, risk mitigation, and risk communication strategies.
• Collaborate with cross-functional teams and stakeholders to ensure that all platforms meet safety, efficacy, quality, and robust supply standards.
• Develop and maintain strong relationships with internal stakeholders to facilitate effective technical support.
• Develop and maintain key performance indicators (KPIs) to measure and improve the effectiveness of COE support.
• Remain informed of current Good Manufacturing Practices (cGMP) and Good Distribution Practices (cGDP) and requirements and industry trends.

Director, Global Distribution Engineering – Technology

Manager

• Contribute to evidence generation across Specialty, General Pharma, and Infectious Diseases
• Support the design, execution, and delivery of real-world evidence and outcomes research studies
• Apply epidemiology, HEOR, and pharmacoepidemiology methods
• Communicate study results through scientific abstracts, peer-reviewed publications, and presentations
• Provide scientific mentorship and support collaborative project execution.

Outcomes Research Manager – Latin America

Project Manager

• Lead cross-functional teams to deliver technology transfers for new veterinary biopharmaceutical products from R&D into commercial manufacturing
• Partner closely with manufacturing sites, R&D, PTS/ATS, Quality, Supply Chain and Regulatory Affairs
• Provide technical leadership throughout the transfer lifecycle, including technical reviews and product and process risk assessments
• Support regulatory submission activities with high-quality technical documentation
• Drive effective project execution through planning of budgets, timelines, resources, and milestones
• Help shape and strengthen best practices, standards, and ways of working within your expertise
• Lead technical investigations and problem-solving activities
• Communicate project progress, risks, and key decisions to senior stakeholders
• Maintain oversight of project schedules, risks and issue registers, and escalate proactively

Project Manager – Tech Transfer

• Reporting directly to the Head of their assigned functional area and acting as a member of their Leadership Team
• Leads global geographic strategy and performance across assigned region / geography
• Responsible for translating functional area and GDMS strategic imperatives into region-specific priorities and plans
• Partners with GDMS and GCTO leaders to drive global alignment, standardization, and transformation of data-management practices
• Represents their function and geography network in GDMS LT forums, and ensures resource excellence, capability growth, and operational readiness worldwide
• Collaborates with cross-functional (non-GDMS) leadership and enterprise support functions within assigned geographies to achieve strategic and operational goals and objectives
• Embeds process-excellence and governance frameworks across regions
• Shapes and implements digitally enabled operating models; drives global alignment, standardization, and transformation
• Champions a culture of collaboration, innovation, and accountability across the network; ensures ongoing improvement and operational excellence
• Partners with leaders across GDMS, GCTO, and Global Clinical Development (GCD) to drive consistent rollout / adoption of capabilities
• Oversees performance governance, financial discipline, and global talent planning; sponsors leadership development and succession
• Ensures consistent operational execution, quality, and compliance across assigned geographies

Executive Director – Clinical Data Management

Sales

• Asegurar el cumplimiento de los objetivos de ventas de la zona
• Promover y posicionar productos y plataformas de servicio
• Desarrollar el plan de acción y promoción de su territorio
• Participar activamente con el Gerente Comercial en los procesos de negociación
• Implementar exitosamente programas de capacitación técnica

Representante Ventas, Salud Animal

Full-stack Engineer

• Design, configure and implement Kinaxis Maestro based on business requirements, translating needs into detailed software specifications that meet user stories and deadlines
• Join supply chain planning design sessions focused on demand/supply planning and order scheduling to shape solution requirements
• Lead data integration and transformation efforts, manage QA/UAT, and collect user feedback to improve implementations
• Coordinate with Kinaxis product engineering, professional services, and support to drive product enhancements
• Run deployment workshops and train/support end users during testing to ensure smooth adoption

Senior Software Engineer

• Act as the Master Data subject matter expert and apply advanced knowledge to the creation, maintenance, review, analysis, and accuracy of master data
• Design, implementation, sustainment, performance, and monitoring of standard business processes in all production execution and master data functions
• Own and drive master data governance activities, including definition of data standards, stewardship roles, and escalation paths
• Gather, analyze, and report process performance and transactional discipline metrics to ensure compliance and continuous improvement; translate metrics into action plans
• Collaborate with other site and regional/global team members and participate as a member of the site CoP Team; influence regional master data strategies
• Develop and maintain SOPs along with associated trainings and provide delivery of the end user trainings; lead change management activities
• Identify, troubleshoot, and resolve complex master data issues and lead root cause corrective actions
• Lead and assist in process improvement projects; manage project planning, stakeholder engagement, and delivery of outcomes
• Identify and implement continuous process improvement opportunities and promote best practices across the network
• Act as a resource for technical expertise—offering consultation, coaching, and practical support to team members at all levels

Senior Specialist, Engineering

• Participates on the Clinical Trial Team (CTT) and collaborates closely with other functional area representatives to negotiate timelines and strategy for clinical supplies.
• Interacts with key partners in both GCS (Logistics and Trade, Distribution, Operations etc.) as well as other organizations such as Global Clinical Trial Operations (GCTO) headquarters and regional colleagues and Global Development Quality (GDQ) to address clinical supply related topics.
• Responsible and accountable for establishing the timelines for clinical supply needs per protocol and ensuring a robust signal for packaging and distribution for Clinical Finished Goods (CFGs)
• Analyzes and anticipates clinical study risks as they relate to clinical supply chain deliverables and prepares, analyzes, and/or develops mitigation strategies for review with clinical partners and senior leaders.
• Responsible and accountable for utilizing key tools/systems such as IRT & Microsoft PowerApps, SWMS, Veeva, MEDS, MyLearning, and other Microsoft Applications in the management of clinical supplies for assigned studies.
• Works directly in the SAP system to ensure a robust and consolidated forecast for CFGs is maintained.
• Report clinical supply chain incidents to support the gathering of metrics in GCS to describe business health.
• Participate in root causing to identify areas for operational improvement.
• Participates in initiation and timely processing of change controls through collaboration with GCS Planning and other cross functional stakeholders and in accordance with established GCS planning SOPs/BPs and QMS Topic 3.4 Change Control Procedures and Work Instructions.
• Participates in authoring and timely processing of deviation records as well as supports deviation investigations as required.
• Participates in critical non-pipeline and compliance activities in support of GCS Planning.
• Participates in supporting regulatory agency inspections for assigned trials as required.
• Demonstrates high capability to solve unstructured problems, make informed risk decisions considering both technical & business risks, & influence portfolio decisions with facts and data.
• Demonstrates ability to balance strategy with ability for tactical execution and has strong ownership & accountability of assigned work.
• Focus on Customers & Patients. Make rapid, disciplined decisions. Demonstrates Ethics & Integrity.

Senior Specialist, Clinical Supply Project Manager – Inventory Manager

Vice President

• Serves as the global head of the Infectious Disease & Vaccines Clinical Scientist function.
• Define and maintain clear role delineation between Clinical Scientists and Clinical Directors.
• Establish expectations for scientific rigor, judgment, and decision making appropriate to phase, modality, and risk.
• Continually optimize organizational design, role clarity, and resourcing for Clinical Scientists aligned with portfolio priorities.
• Own the clinical scientist framework for Infectious Disease & Vaccines studies.
• Provide senior scientific input into data interpretation for clinical outcomes, safety signal evaluation, and benefit risk assessments.
• Act as a senior scientific partner to Therapeutic Area Heads and Clinical Development leadership.
• Represent the Clinical Scientist function in governance forums and review committees.
• Partner closely with Clinical Trial Operations teams ensuring seamless work between clinical and operations.
• Ensure robust performance management, coaching, and career development processes are implemented by CS people leaders.

AVP, Head of Infectious Disease & Vaccines Clinical Science

Clinical Research

• Provide leadership and experience in conducting early clinical research in China.
• Develop products towards registration, including study protocol, engaging key opinion leaders, drafting study reports, and preparing regulatory submissions.
• Collaborate with headquarter project teams and clinical trial operations for the execution of early studies.
• Represent clinical development team and address issues/questions raised by headquarters team from China perspective.
• Drive study design, collaborate with biostatisticians and regulatory affairs to construct high-quality clinical study protocols.
• Review and prepare clinical study reports and regulatory dossiers.

Senior Manager, Clinical Research

• Perform advanced configuration, integrations, data transformation, release support and L3-style troubleshooting across a large, multi-module Enablon environment (20,000+ users, multiple customizations and integrations).
• Implement and maintain advanced Enablon configurations: rules engine, notifications, workflows, conditional fields, settings tables, sub-forms and other platform features.
• Work from tickets escalated by L1/L2 after initial analysis; provide clear time estimates before starting Level 3 work.
• Own Level 3 tickets through analysis, build/configure, unit testing, packaging and handoff for production deployment.
• Contribute to and maintain SOPs, runbooks, SLAs and support playbooks to improve in-house support maturity.
• Design, develop and maintain integrations between Enablon and central data lake / third-party systems; perform mapping, remapping and significant integration revisions.

Senior Specialist, Software Engineering

• Collaborate with Product team to own the end-to-end lifecycle for core clinical development systems (~10 systems including IRT/RTSM, EDC, Medical Review, CTMS, eTMF, PV database, statistics & analysis platform, Data Room, project management, eCOA/ePRO).
• Defines product vision, strategy, and roadmap aligned to clinical development objectives, compliance requirements, and user experience; establishes OKRs/KPIs for value realization.
• Leads demand intake and prioritization with business stakeholders; makes product decisions and trade-offs to maximize patient safety, data integrity, delivery predictability, and total cost of ownership.
• Understands end-to-end clinical R&D processes and anticipates evolving needs (e.g., decentralized trials, real-time data review, automation, and analytics enablement).
• Defines and monitors product metrics (adoption, incident/defect trends, system performance/availability, cycle time).
• Drive continuous discovery with Clinical Ops to uncover pain points and translate them into requirements, user stories, and solution options.
• Maintains a prioritized backlog and release plan; owns cross-system dependency management and end-to-end integration delivery.
• Drives user adoption and change management: training enablement, communications, SOP/process updates.
• Leads release, validation/compliance, and support planning to ensure stable operations and inspection readiness.
• Acts as the primary interface between business stakeholders, IT delivery/operations, and external vendors; facilitates clear communication, issue resolution, and timely decisions.
• Manages product financials and vendor contracts; continuously optimizes operating model and total cost of ownership.
• Ensures fit-for-purpose governance and documentation in partnership with QA/Compliance and IT.

MSD