Marketing

• Resolve questions and concerns effectively and efficiently by actively listening, communicating clearly, and assuring understanding of the question/issue.
• Respond to our company National Service Center and Field Service Center inquiries using knowledge base documents, Prescribing Information/Medication Guide documents, and databases.
• Provide off-label scientific/medical information to Healthcare Professionals in response to unsolicited inquires.
• Document interactions, recording details of inquiries, complaints, comments and actions taken, to include intake of Adverse Events and Product Quality Complaints.
• Ensures the delivery of the desired customer experience for all customer/employee engagements.
• May manage development and execution of customer/consumer/employee multi-channel communications, workflow processes, and operating procedures to ensure effective and efficient contact center operations and consistent delivery of the desired customer experience.
• May collaborate with internal stakeholders to develop and execute changes in processes/ procedures, plan and implement new strategies, share status of operations and key performance metrics, and manage escalated issues.
• Manage escalated customer requests to resolution for assigned projects, and assess customer interactions to continually enhance the customer experience and achieve operational excellence.

Senior Specialist, Shared Services Marketing

Clinical Research

• Provide statistical support to projects in the BARDS HTA Statistics group, including HTA submissions
• Contribute to the design and development of scientific tools for HTA evaluations
• Execute on ongoing HTA evaluations, including analysis and interpretation of HTA results
• Collaborate with Statistical Programming to implement methodologies and ensure high quality deliverables for HTA submissions
• Prepare written reports to effectively communicate results of HTA evaluations to the Value & Implementation Observational Research (VIOR) and subsidiary teams

Biostatistician

Medical Director

• Develops ongoing professional relationships with key decision makers in organized health systems to ensure access to medical and scientific information on the full product portfolio and areas of therapeutic interest
• Develops strategic account plans in partnership with the Integrated Account Management (IAM) Account Executive teams and executes medical activities in alignment with agreed plan
• Serves as the primary resource for market dynamics within the territory to understand decision makers’ evolving information needs to feed into the ongoing value-proposition development process for product and non-product offerings
• Effectively communicates and coordinates with Regional Medical Scientific Director (RMSD) regarding medical and scientific support needs in key health systems accounts
• Serves as a resource for the HS MAD Team Lead, HS Executive Director Medical Affairs, and other members of Country Medical Affairs on other relevant strategic planning
• Attends and supports scientific and medical meetings and prepares post-meeting deliverables

Regional Health Systems Medical Affairs Director

Account Executive

• As a Sr. Chronic Care Specialty Sales Representative, you will drive meaningful patient impact by leveraging our scientific expertise and serving as the primary contact for customers within your assigned territory.
• Collaborate closely with Account Executives, Integrated Delivery Systems leaders, and other field colleagues to deliver seamless, patient-focused solutions.
• Develop and execute a territory-level business plan in alignment with company policies, standards, and ethics.
• Maintain current product knowledge and certifications for the company’s portfolio.
• Conduct balanced and compliant product sales discussions with health care providers and business professionals to align customer needs with company products according to product labeling.
• Provide management with regular updates on customer needs, marketplace dynamics, and progress toward quality goals.
• Be knowledgeable on headquarter approved information regarding approved company products, disease, and marketplace.
• Monitor business performance against objectives using company tools to support effective planning and sales impact.

Senior Chronic Care Specialty Sales Representative

Operations

• work as a part of the integrated Stability Operations & Compliance team and drive a culture of quality and operational excellence across the global AR&D network
• oversee and manage end to end GMP stability studies and logistics for our large molecule portfolio
• collaborate in a fast-paced, integrated, multidisciplinary team environment
• support the identification of internal and external stability sites and assess capabilities and capacity
• participate in cross-functional teams for vaccines, biologics, and/or devices for the management of clinical and commercial GMP stability studies
• plan, coordinate across internal and external networks, and implement stability studies for the large molecule portfolio
• manage GMP documentation including stability protocols, Standard Operating Procedures (SOP), Re-evaluation dating memo, Stability reports and GMP data
• successful collaboration with internal and external parties to ensure implementation and execution of stability studies
• ensure coordination with stability staging and testing laboratories for efficient sample and data management
• track stability metrics to ensure pull-on-time, test-on-time and review-on-time
• utilize Digital applications (such as Electronic Data Management Systems, Laboratory Information Management System) for stability study builds and data management
• support second person review requirements to ensure accuracy, compliance, integrity, completeness, and traceability of stability documentation
• maintain accurate records including sample inventory and sample chain of custody
• evaluate stability data, including statistical analysis and trending, investigating out-of-specification stability results
• communicate with integrated project teams for biologics, vaccines, and devices
• support authoring regulatory source documents and stability sections
• support re-evaluation dating and associated change controls, address stability-related deviations and investigations, maintain change management records and GMP documentation
• support logistical requirements for capital expansions including facility/CTU requirements and capacity planning
• continuous improvement to maintain state-of-the-art stability infrastructure to meet Global compliance standards

Associate Director – Stability Operations

Security Engineer

• Lead the design, engineering, and scaling of enterprise product security platforms.
• Ensure cloud‑native security patterns are deeply integrated across AWS, Azure, etc environments.
• Conduct technology research to evaluate emerging threats, vulnerabilities, and cloud provider risks.
• Establish and maintain secure architecture standards, configuration baselines, and best practices for cloud and product security platforms.
• Drive modernization and automation of security workflows with a DevSecOps mindset.
• Translate enterprise security strategy and policy into actionable architecture, platform capabilities, and engineering implementations.
• Define security requirements and enable collaborative development of scalable system and service architectures.
• Collaborate on cloud security governance, data protection strategy, and secure adoption frameworks.
• Guide platform teams and developers to close gaps in cloud posture, application security, and data protection maturity.
• Perform Security Assessments using frameworks such as CSA, NIST, PCI, and internal controls.
• Ensure compliance with enterprise risk standards, policies, regulatory expectations, and audit requirements.
• Write code, scripts, and automation to enhance security tooling, dashboards, integrations, and workflows.
• Mentor team members and serve as an escalation point on complex or unusual issues.

Cloud Security Engineer

Procurement

• Manage the CapEx spend from projects up to $5M across all our Company divisions
• Serve as a liaison between the sites and the Global Cap Ex team
• Ensure the correct sourcing and execution of projects and 100% compliance with processes and policies
• Provide primary expertise in Capital sourcing, stakeholder engagement and management and performance improvement of the capital spend
• Develop direct relationships with internal stakeholders and suppliers
• Train stakeholders on our processes and policies
• Collaborate with site teams to understand the Long-range Capital plan
• Build our projects pipeline
• Support the building and approval of Project Procurement Plans (PPPs)
• Lead sourcing projects to deliver optimal value to the company
• Drive increases in varied spend
• Perform supplier negotiations to support projects
• Monitor key suppliers through agreed KPIs and perform Quarterly Business Reviews
• Develop, support, and execute a comprehensive regional and local strategy in line with the global strategy
• Stay at the forefront of sustainability best practices, regulations, and industry trends

Senior Specialist – Regional Cap Ex Procurement

Data Analyst

• Assists the V&I organization in discovering information hidden in data to make data driven strategic decisions.
• 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 and a strong understanding of healthcare data and technology.
• Keeps abreast of the latest trends in the field through continuous learning and proactively championing new methods to help solve critical and emerging V&I problems.
• Collaborates and partners with peers in other functions on cross-functional analytics projects.
• Manages external vendors.
• Develops and owns scalable-analytic products that fulfill stakeholders needs.

Associate Director – Value & Implementation, Medical Data Analytics, Data Enablement

Software Engineer

• Provides oversight and quality management of submission data standard deliverables for world-wide regulatory application submissions of drug and vaccine clinical development projects.
• Accountability predominantly includes submission data standards planning activities, coaching and consulting with project teams, outreach to external vendors and partners, and keeping current with industry submission data standards including SDTM, ADaM, clinical site data for CDER inspection planning, etc.
• Responsible for continuous improvement of our electronic submission process and providing tools and templates to support delivery focusing on traceability, quality assurance, data conformance and data fitness.
• Key collaborator with statistical programming, statistics, regulatory and other project stakeholders
• PreNDA and PreBLA meeting preparation, study data standards plan, preparing questions for FDA e-data mailboxes (CBER/CDER), attendance at meetings with regulatory agencies (FDA, EMA, PMDA)
• Guiding project teams preparing submission deliverables including use of Pinnacle 21 Enterprise Up-versioning activities to specific versions of SDTM
• Participation in industry teams and conferences on best practices
• Membership on departmental strategic initiative project teams

Senior Scientist, Statistical Programmer, Submission Data Standards Quality Management

• Lead design, development, and scaling of product security platforms, including integrating application scanners and cloud-native security guardrails
• Integrate security controls into CI/CD pipelines, provisioning workflows, and developer platforms
• Drive automation/AI and orchestration to reduce manual security review overhead
• Translate enterprise security policies and standards into enforceable platform capabilities
• Partner with architecture, Cloud, DevOps, and product teams to integrate secure‑by‑design principles into engineering workflows
• Establish platform KPIs, KRIs, and adoption metrics; enable reporting for risk reviews, leadership updates, and regulatory needs
• Oversee platform operations, including performance, availability, team processes, backlog management, vendor management, and escalations
• Lead a team of platform engineers and security specialists
• Provide mentorship, career development, and continuous learning opportunities
• Work closely with product lines, cloud engineering, DevOps, and enterprise security teams to drive adoption of platform capabilities

Associate Director, Cybersecurity Engineering

Research Scientist

• This position resides within our company's Value and Implementation (V&I), Outcomes Research organization, which is responsible for real-world evidence generation and outcomes research studies to enable sustained patient access to our company’s innovations and improve patient health outcomes.
• Under the guidance of a senior leader, this individual will support the V&I, Outcomes Research teams supporting Oncology Asset(s).
• Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling.
• The incumbent is expected to contribute to product development and marketing strategies throughout the lifecycle to ensure that product value is defined and developed to achieve optimal market/patient access and reimbursement.
• The incumbent is expected to work cross-functionally with clinical development, medical affairs, biostatistics, market access, commercial and country affiliates and may have direct interactions with health technology assessment (HTA) agencies, reimbursement decision makers and national immunization technical advisory groups.

Principal Scientist – Outcomes Research, Oncology Asset

Director

• 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
• Ensures robust two-way communication with U.S., China, and Japan Executive Directors (Eds) or equivalents
• Captures market-specific needs and insights to inform global strategy, while also guiding local execution in alignment with global V&I plans
• Integrates into the EDMA Tandem model to foster strategic clarity and executional excellence
• Partners with U.S. EDMA and Health Systems EDs to align payor strategies, precision-medicine initiatives, and congress deliverables
• Ensures team contributes as relevant members to the PDT and/or ADT sub-teams (V&I, Value Evidence, Clinical, Commercial, Publications, and Label teams)
• Applies expertise in country’s medical systems and clinical practice standards to guide Global Directors Medical Affairs (GDMAs) and/or Regional Directors Medical Affairs (RDMAs) and partners with Regional Strategy Leads (RSLs) to anticipate challenges, identify solutions, and implement actions that support adoption of new innovations

Executive Director, Medical Affairs, Genitourinary

• Leading the commercial strategy development for specific indications for sac-TMT (TBD)
• Driving the development of indication-level L3 and other marketing strategy-related asset deliverables, scientific narrative and any relevant unbranded strategy work, 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 relevant indications
• Includes coordination with precision medicine team on biomarker strategies related to relevant indications
• Leading commercial planning and execution for relevant indications for sac-TMT
• Development of promotional strategies, messaging and any necessary global content deliverables, in collaboration with relevant disease 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 for relevant indication-level work, ensuring close cross-functional and cross-geographic coordination
• SL engagement/congress strategy for relevant launch indications, in coordination with relevant disease teams and broader sac-TMT asset planning workstreams
• Data analytics, performance metrics tracking for relevant indications, in close coordination with relevant disease teams and sac-TMT analytics team
• Coordination with precision medicine team on commercialization of TROP2 CDx for relevant indications
• Preparation for launch readiness and other governance discussions related to the relevant indications of sac-TMT
• Coaching, guiding and development of direct reports, gig assignments, etc

Director, Global Oncology Marketing

• Lead digital projects: Identify, evaluate, and implement enterprise-level Environmental Health and Safety digital solutions, including replacing systems at end of life and staying current with emerging technologies and industry trends.
• Partner with information technology: Build strong relationships to ensure smooth implementation, sustainment, and continuous improvement of EHS systems.
• Improve adoption and skills: Use data to spot user skill gaps and design targeted training and engagement to boost system adoption and performance.
• Drive continuous improvement: Develop and refine procedures, guidelines, and training to keep EHS digital systems optimized and aligned with best practices.
• Build business cases: Quantify benefits and return on investment to secure resources and stakeholder support for enhancements and new solutions.
• Coach leaders: Enable leaders across functions to successfully adopt and use digital EHS solutions.
• Communicate and present: Create clear, compelling presentations and updates for senior management and stakeholders.
• Manage projects: Serve as project manager or key team member for initiatives requiring EHS subject matter expertise and systems support.
• Track metrics: Monitor compliance, performance metrics, and feedback; lead the consolidation of company-wide EHS metrics to inform decision-making.
• Collaborate externally: Engage with peer organizations to learn from the market and identify future opportunities in EHS digital systems.
• Lead the team: Manage, mentor, and develop a team of EHS professionals, fostering an inclusive, growth-oriented environment.

Associate Director, EHS Digital Portfolio Management

• Coach and mentor junior scientists, fostering their professional growth and development within the organization.
• Lead Human Factors Project Work (Strategy and Execution), including, but not limited to Own HF strategy from early concept through validation and post-market for devices and combination products.
• Build HF plans and study roadmaps; select methods (user research, task/use-error analysis, risk mitigation, formative/summative usability testing).
• Turn user insights into design inputs for device UI, packaging, labeling, and IFU; guide intuitive, safe designs.
• Partner with marketing, program management, clinical, safety, regulatory, manufacturing, packaging, and labeling to integrate HF and manage risk.
• Lead regulatory deliverables: HF protocols/reports, linkage to risk management (ISO 14971), hazard/use-related risk analyses, and submission materials (FDA, EU MDR).
• Maintain compliant HF documentation and traceability; ensure audit readiness.
• Monitor post-market use-related issues and drive corrective actions and training.
• Define and continuously improve HF process, standards, and templates per IEC 62366-1 and FDA guidance.
• Set clear governance (gates, criteria, documentation) for consistent HF quality across programs.
• Create reusable methods for needs discovery, user profiling, task analysis, and use-related risk assessment.
• Provide portfolio-level guidance for UI, labeling, and IFU to reduce use-related risk.
• Train cross-functional teams on HF practices and compliant documentation.
• Establish metrics and feedback loops (study quality, defects, post-market signals) to prioritize improvements.
• Maintain centralized HF libraries and tools to enable reuse and speed development.